DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs1004639863 |
Type: RSID SNP
Position hg183: 9928652
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
20 |
10000004 |
9980652 |
rs949540033 |
Type: RSID SNP
Position hg183: 9928654
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
C |
20 |
10000006 |
9980654 |
rs1238719605 |
Type: RSID SNP
Position hg183: 9928664
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
20 |
10000016 |
9980664 |
rs1046607306 |
Type: RSID SNP
Position hg183: 9928678
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
C |
20 |
10000030 |
9980678 |
rs1330805844 |
Type: RSID SNP
Position hg183: 9928682
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
20 |
10000034 |
9980682 |
rs1385045321 |
Type: RSID SNP
Position hg183: 9928690
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
20 |
10000042 |
9980690 |
rs1389717752 |
Type: RSID SNP
Position hg183: 9928702
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
20 |
10000054 |
9980702 |
rs566536121 |
Type: RSID SNP
Position hg183: 9928703
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
20 |
10000055 |
9980703 |
rs1426346129 |
Type: RSID SNP
Position hg183: 9928705
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
20 |
10000057 |
9980705 |
rs373926720 |
Type: RSID SNP
Position hg183: 9928706
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
A |
20 |
10000058 |
9980706 |
