rs41546617

Orientation

minus

Stabilized

minus

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

Make rs41546617(G;G)

Make rs41546617(G;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31356938

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs41546617
dbSNP (classic)	rs41546617
ClinGen	rs41546617
ebi	rs41546617
HLI	rs41546617
Exac	rs41546617
Gnomad	rs41546617
Varsome	rs41546617
LitVar	rs41546617
Map	rs41546617
PheGenI	rs41546617
Biobank	rs41546617
1000 genomes	rs41546617
hgdp	rs41546617
ensembl	rs41546617
geneview	rs41546617
scholar	rs41546617
google	rs41546617
pharmgkb	rs41546617
gwascentral	rs41546617
openSNP	rs41546617
23andMe	rs41546617
SNPshot	rs41546617
SNPdbe	rs41546617
MSV3d	rs41546617
GWAS Ctlg	rs41546617

Max Magnitude

0

ClinVar
Risk	rs41546617(C;C) rs41546617(G;G)
Alt	rs41546617(C;C) rs41546617(G;G)
Reference	Rs41546617(T;T)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31324715A>C; NC_000006.11:g.31324715A>G
CLNSRC
CLNACC