DNA Marker Index data
Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs1468373888 |
Type: RSID SNP
Position hg183: 51000
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
T |
19 |
100000 |
100000 |
rs769522595 |
Type: RSID SNP
Position hg183: 950999
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
19 |
1000000 |
999999 |
rs1037395275 |
Type: RSID SNP
Position hg183: 9971678
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
19 |
10000002 |
10110678 |
rs897606705 |
Type: RSID SNP
Position hg183: 9971681
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
19 |
10000005 |
10110681 |
rs1344673050 |
Type: RSID SNP
Position hg183: 9971685
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
19 |
10000009 |
10110685 |
rs1238870071 |
Type: RSID SNP
Position hg183: 951000
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
19 |
1000001 |
1000000 |
rs188767851 |
Type: RSID SNP
Position hg183: 9971687
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
19 |
10000011 |
10110687 |
rs893846567 |
Type: RSID SNP
Position hg183: 9971692
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
19 |
10000016 |
10110692 |
rs1278355202 |
Type: RSID SNP
Position hg183: 9971693
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
19 |
10000017 |
10110693 |
rs1025772833 |
Type: RSID SNP
Position hg183: 9971694
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
19 |
10000018 |
10110694 |