DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs1164068588 |
Type: RSID SNP
Position hg183: 9844243
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
AC |
A |
17 |
10000201 |
9903518 |
rs1384012538 |
Type: RSID SNP
Position hg183: 9844243
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
ACCC |
A |
17 |
10000201 |
9903518 |
rs1181679191 |
Type: RSID SNP
Position hg183: 9844244
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
17 |
10000202 |
9903519 |
rs1445337746 |
Type: RSID SNP
Position hg183: 850011
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
17 |
1000021 |
903261 |
rs118142575 |
Type: RSID SNP
Position hg183: 9844252
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
17 |
10000210 |
9903527 |
rs1446323199 |
Type: RSID SNP
Position hg183: 9844271
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
17 |
10000229 |
9903546 |
rs952276034 |
Type: RSID SNP
Position hg183: 9844272
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
17 |
10000230 |
9903547 |
rs746966068 |
Type: RSID SNP
Position hg183: 9844280
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
17 |
10000238 |
9903555 |
rs951748053 |
Type: RSID SNP
Position hg183: 9844290
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
A,C |
17 |
10000248 |
9903565 |
rs1172806243 |
Type: RSID SNP
Position hg183: 9844115
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
17 |
10000073 |
9903390 |
