rs41559413

Orientation

minus

Stabilized

minus

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

Make rs41559413(C;C)

Make rs41559413(C;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31356559

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs41559413
dbSNP (classic)	rs41559413
ClinGen	rs41559413
ebi	rs41559413
HLI	rs41559413
Exac	rs41559413
Gnomad	rs41559413
Varsome	rs41559413
LitVar	rs41559413
Map	rs41559413
PheGenI	rs41559413
Biobank	rs41559413
1000 genomes	rs41559413
hgdp	rs41559413
ensembl	rs41559413
geneview	rs41559413
scholar	rs41559413
google	rs41559413
pharmgkb	rs41559413
gwascentral	rs41559413
openSNP	rs41559413
23andMe	rs41559413
SNPshot	rs41559413
SNPdbe	rs41559413
MSV3d	rs41559413
GWAS Ctlg	rs41559413

Max Magnitude

0

ClinVar
Risk	rs41559413(C;C)
Alt	rs41559413(C;C)
Reference	Rs41559413(G;G)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31324336C>G
CLNSRC
CLNACC