DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs569613325 |
Type: RSID SNP
Position hg183: 9990000
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
C |
18 |
10000003 |
10000000 |
rs745318691 |
Type: RSID SNP
Position hg183: 9990001
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
18 |
10000004 |
10000001 |
rs924291826 |
Type: RSID SNP
Position hg183: 9990002
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
18 |
10000005 |
10000002 |
rs994983768 |
Type: RSID SNP
Position hg183: 990002
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
G |
18 |
1000001 |
1000002 |
rs1446950547 |
Type: RSID SNP
Position hg183: 9990008
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
18 |
10000011 |
10000008 |
rs1244336540 |
Type: RSID SNP
Position hg183: 9990015
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
18 |
10000018 |
10000015 |
rs538147077 |
Type: RSID SNP
Position hg183: 9990021
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
18 |
10000024 |
10000021 |
rs540652508 |
Type: RSID SNP
Position hg183: 9990022
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
18 |
10000025 |
10000022 |
rs976378999 |
Type: RSID SNP
Position hg183: 9990025
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
18 |
10000028 |
10000025 |
rs1476444250 |
Type: RSID SNP
Position hg183: 990004
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
T |
18 |
1000003 |
1000004 |
