DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs1425019419 |
Type: RSID SNP
Position hg183: 99376078
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
11 |
100000136 |
99870868 |
rs966922746 |
Type: RSID SNP
Position hg183: 99376079
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
11 |
100000137 |
99870869 |
rs999673929 |
Type: RSID SNP
Position hg183: 99376080
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
11 |
100000138 |
99870870 |
rs1032528130 |
Type: RSID SNP
Position hg183: 99376081
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
11 |
100000139 |
99870871 |
rs1469186425 |
Type: RSID SNP
Position hg183: 99376087
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
11 |
100000145 |
99870877 |
rs1428704686 |
Type: RSID SNP
Position hg183: 99376089
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
TA |
11 |
100000147 |
99870879 |
rs1401405124 |
Type: RSID SNP
Position hg183: 99376090
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
AAAGTAT |
A |
11 |
100000148 |
99870880 |
rs189487937 |
Type: RSID SNP
Position hg183: 9978138
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
11 |
10000015 |
10021562 |
rs1161334713 |
Type: RSID SNP
Position hg183: 99376094
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
TATAATA |
T |
11 |
100000152 |
99870884 |
rs916260251 |
Type: RSID SNP
Position hg183: 99375999
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
11 |
100000057 |
99870789 |
rs183347912 |
Type: RSID SNP
Position hg183: 99375997
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
11 |
100000055 |
99870787 |
rs1388105931 |
Type: RSID SNP
Position hg183: 99375990
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
11 |
100000048 |
99870780 |
rs575337831 |
Type: RSID SNP
Position hg183: 99375984
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
11 |
100000042 |
99870774 |
rs1344294011 |
Type: RSID SNP
Position hg183: 99375983
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
11 |
100000041 |
99870773 |
rs12800033 |
Type: RSID SNP
Position hg183: 99375981
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
T |
11 |
100000039 |
99870771 |
rs1400138239 |
Type: RSID SNP
Position hg183: 99375977
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
11 |
100000035 |
99870767 |
rs1280647429 |
Type: RSID SNP
Position hg183: 99375975
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
11 |
100000033 |
99870765 |
rs925064563 |
Type: RSID SNP
Position hg183: 99375968
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
C |
11 |
100000026 |
99870758 |
rs978223771 |
Type: RSID SNP
Position hg183: 99375967
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
11 |
100000025 |
99870757 |
rs1020056324 |
Type: RSID SNP
Position hg183: 99375965
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A,C |
11 |
100000023 |
99870755 |