rs41559422

Orientation

minus

Stabilized

minus

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

Make rs41559422(C;T)

Make rs41559422(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31355890

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs41559422
dbSNP (classic)	rs41559422
ClinGen	rs41559422
ebi	rs41559422
HLI	rs41559422
Exac	rs41559422
Gnomad	rs41559422
Varsome	rs41559422
LitVar	rs41559422
Map	rs41559422
PheGenI	rs41559422
Biobank	rs41559422
1000 genomes	rs41559422
hgdp	rs41559422
ensembl	rs41559422
geneview	rs41559422
scholar	rs41559422
google	rs41559422
pharmgkb	rs41559422
gwascentral	rs41559422
openSNP	rs41559422
23andMe	rs41559422
SNPshot	rs41559422
SNPdbe	rs41559422
MSV3d	rs41559422
GWAS Ctlg	rs41559422

GMAF

0.02479

Max Magnitude

0

ClinVar
Risk	rs41559422(T;T)
Alt	rs41559422(T;T)
Reference	Rs41559422(C;C)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31323667G>A
CLNSRC
CLNACC