DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs117121855 |
Type: RSID SNP
Position hg183: 10001365
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
16 |
10000007 |
10093864 |
rs1160132317 |
Type: RSID SNP
Position hg183: 990002
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A,T |
16 |
1000001 |
1050001 |
rs1363427324 |
Type: RSID SNP
Position hg183: 10001375
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
16 |
10000017 |
10093874 |
rs542452687 |
Type: RSID SNP
Position hg183: 10001383
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
16 |
10000025 |
10093882 |
rs560025441 |
Type: RSID SNP
Position hg183: 990004
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
16 |
1000003 |
1050003 |
rs1473577832 |
Type: RSID SNP
Position hg183: 10001389
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
16 |
10000031 |
10093888 |
rs562218031 |
Type: RSID SNP
Position hg183: 10001394
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
16 |
10000036 |
10093893 |
rs1256045614 |
Type: RSID SNP
Position hg183: 10001400
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
CCT |
C |
16 |
10000042 |
10093899 |
rs1210742168 |
Type: RSID SNP
Position hg183: 10001403
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
CTGT |
C |
16 |
10000045 |
10093902 |
rs997179954 |
Type: RSID SNP
Position hg183: 10001410
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
16 |
10000052 |
10093909 |
