DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs1411921275 |
Type: RSID SNP
Position hg183: 99363604
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
5 |
100000001 |
99335705 |
rs1272324943 |
Type: RSID SNP
Position hg183: 99363610
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
5 |
100000007 |
99335711 |
rs443601 |
Type: RSID SNP
Position hg183: 10053113
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
5 |
10000001 |
10000113 |
rs1015051799 |
Type: RSID SNP
Position hg183: 99363613
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
5 |
100000010 |
99335714 |
rs1451764797 |
Type: RSID SNP
Position hg183: 99363620
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
5 |
100000017 |
99335721 |
rs1351293608 |
Type: RSID SNP
Position hg183: 99363625
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
CACTT |
C |
5 |
100000022 |
99335726 |
rs897904105 |
Type: RSID SNP
Position hg183: 99363631
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
5 |
100000028 |
99335732 |
rs1312462158 |
Type: RSID SNP
Position hg183: 99363642
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
A |
5 |
100000039 |
99335743 |
rs965816088 |
Type: RSID SNP
Position hg183: 99363647
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
C |
5 |
100000044 |
99335748 |
rs1404441982 |
Type: RSID SNP
Position hg183: 99363653
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
A |
5 |
100000050 |
99335754 |
