DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs894831941 |
Type: RSID SNP
Position hg183: 9844043
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
17 |
10000001 |
9903318 |
rs973399740 |
Type: RSID SNP
Position hg183: 9844044
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
17 |
10000002 |
9903319 |
rs1445930213 |
Type: RSID SNP
Position hg183: 9844045
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
A |
17 |
10000003 |
9903320 |
rs1258976558 |
Type: RSID SNP
Position hg183: 9844048
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
17 |
10000006 |
9903323 |
rs917423623 |
Type: RSID SNP
Position hg183: 9844050
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
17 |
10000008 |
9903325 |
rs563665304 |
Type: RSID SNP
Position hg183: 9844051
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
17 |
10000009 |
9903326 |
rs1044443503 |
Type: RSID SNP
Position hg183: 9844052
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
17 |
10000010 |
9903327 |
rs927404198 |
Type: RSID SNP
Position hg183: 9844054
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
17 |
10000012 |
9903329 |
rs1055190296 |
Type: RSID SNP
Position hg183: 849992
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
17 |
1000002 |
903242 |
rs1221430474 |
Type: RSID SNP
Position hg183: 9844062
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
G |
17 |
10000020 |
9903337 |
