DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs897828841 |
Type: RSID SNP
Position hg183: 9990303
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
18 |
10000306 |
10000303 |
rs1340072720 |
Type: RSID SNP
Position hg183: 9990305
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
18 |
10000308 |
10000305 |
rs569463073 |
Type: RSID SNP
Position hg183: 9990306
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
18 |
10000309 |
10000306 |
rs190972890 |
Type: RSID SNP
Position hg183: 9990307
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A,T |
18 |
10000310 |
10000307 |
rs1035690660 |
Type: RSID SNP
Position hg183: 9990312
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
18 |
10000315 |
10000312 |
rs895760913 |
Type: RSID SNP
Position hg183: 9990325
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
18 |
10000328 |
10000325 |
rs552150732 |
Type: RSID SNP
Position hg183: 9990331
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
18 |
10000334 |
10000331 |
rs2212497 |
Type: RSID SNP
Position hg183: 9990332
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
18 |
10000335 |
10000332 |
rs968559187 |
Type: RSID SNP
Position hg183: 9990334
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
C |
18 |
10000337 |
10000334 |
rs1320122591 |
Type: RSID SNP
Position hg183: 9990156
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
18 |
10000159 |
10000156 |
rs1249008520 |
Type: RSID SNP
Position hg183: 9990137
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
18 |
10000140 |
10000137 |
rs779710707 |
Type: RSID SNP
Position hg183: 9990130
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
18 |
10000133 |
10000130 |
rs1050582793 |
Type: RSID SNP
Position hg183: 9990124
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
18 |
10000127 |
10000124 |
rs933554375 |
Type: RSID SNP
Position hg183: 9990107
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
C |
18 |
10000110 |
10000107 |
rs1284735602 |
Type: RSID SNP
Position hg183: 9990101
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
18 |
10000104 |
10000101 |
rs1384858972 |
Type: RSID SNP
Position hg183: 9990092
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
18 |
10000095 |
10000092 |
rs755753777 |
Type: RSID SNP
Position hg183: 9990091
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
18 |
10000094 |
10000091 |
rs916886561 |
Type: RSID SNP
Position hg183: 9990059
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
18 |
10000062 |
10000059 |
rs562028397 |
Type: RSID SNP
Position hg183: 9990058
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
18 |
10000061 |
10000058 |
rs1000818279 |
Type: RSID SNP
Position hg183: 9990054
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
18 |
10000057 |
10000054 |