rs138659308

Merged into

rs1131201

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs138659308(C;C)

Make rs138659308(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31356765

Gene

HLA-B

is a	snp
is	mentioned by
dbSNP	rs138659308
dbSNP (classic)	rs138659308
ClinGen	rs138659308
ebi	rs138659308
HLI	rs138659308
Exac	rs138659308
Gnomad	rs138659308
Varsome	rs138659308
LitVar	rs138659308
Map	rs138659308
PheGenI	rs138659308
Biobank	rs138659308
1000 genomes	rs138659308
hgdp	rs138659308
ensembl	rs138659308
geneview	rs138659308
scholar	rs138659308
google	rs138659308
pharmgkb	rs138659308
gwascentral	rs138659308
openSNP	rs138659308
23andMe	rs138659308
SNPshot	rs138659308
SNPdbe	rs138659308
MSV3d	rs138659308
GWAS Ctlg	rs138659308

Status

Merged into rs1131201

Max Magnitude

0

ClinVar
Risk	rs138659308(C;C)
Alt	rs138659308(C;C)
Reference	Rs138659308(T;T)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	0
HGVS	NC_000006.11:g.31324542T>C
CLNSRC
CLNACC