DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs1330216714 |
Type: RSID SNP
Position hg183: 9990010
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
9 |
10000010 |
10000010 |
rs1243921313 |
Type: RSID SNP
Position hg183: 101802221
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
9 |
100000118 |
102762400 |
rs1268620521 |
Type: RSID SNP
Position hg183: 101802228
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
C |
9 |
100000125 |
102762407 |
rs927237421 |
Type: RSID SNP
Position hg183: 101802231
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
A |
9 |
100000128 |
102762410 |
rs937330163 |
Type: RSID SNP
Position hg183: 101802247
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
G |
9 |
100000144 |
102762426 |
rs1057172618 |
Type: RSID SNP
Position hg183: 101802254
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A,T |
9 |
100000151 |
102762433 |
rs1344494949 |
Type: RSID SNP
Position hg183: 101802256
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
G |
9 |
100000153 |
102762435 |
rs530674039 |
Type: RSID SNP
Position hg183: 101802257
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
9 |
100000154 |
102762436 |
rs1010328479 |
Type: RSID SNP
Position hg183: 101802269
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
9 |
100000166 |
102762448 |
rs1003500525 |
Type: RSID SNP
Position hg183: 101802270
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
C |
9 |
100000167 |
102762449 |
rs752645711 |
Type: RSID SNP
Position hg183: 101802271
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
9 |
100000168 |
102762450 |
rs1470517932 |
Type: RSID SNP
Position hg183: 9990017
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
9 |
10000017 |
10000017 |
rs1283827877 |
Type: RSID SNP
Position hg183: 101802278
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
9 |
100000175 |
102762457 |
rs551183626 |
Type: RSID SNP
Position hg183: 101802293
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
9 |
100000190 |
102762472 |
rs1398916173 |
Type: RSID SNP
Position hg183: 101802299
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
9 |
100000196 |
102762478 |
rs1373513563 |
Type: RSID SNP
Position hg183: 101802300
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
9 |
100000197 |
102762479 |
rs548112803 |
Type: RSID SNP
Position hg183: 101802311
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
9 |
100000208 |
102762490 |
rs1431107045 |
Type: RSID SNP
Position hg183: 101802314
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
CA |
C |
9 |
100000211 |
102762493 |
rs1310494577 |
Type: RSID SNP
Position hg183: 101802322
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
9 |
100000219 |
102762501 |
rs1382451638 |
Type: RSID SNP
Position hg183: 101802324
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
G |
9 |
100000221 |
102762503 |