rs137854671

Orientation

minus

Stabilized

minus

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

Make rs137854671(C;G)

Make rs137854671(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31356839

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs137854671
dbSNP (classic)	rs137854671
ClinGen	rs137854671
ebi	rs137854671
HLI	rs137854671
Exac	rs137854671
Gnomad	rs137854671
Varsome	rs137854671
LitVar	rs137854671
Map	rs137854671
PheGenI	rs137854671
Biobank	rs137854671
1000 genomes	rs137854671
hgdp	rs137854671
ensembl	rs137854671
geneview	rs137854671
scholar	rs137854671
google	rs137854671
pharmgkb	rs137854671
gwascentral	rs137854671
openSNP	rs137854671
23andMe	rs137854671
SNPshot	rs137854671
SNPdbe	rs137854671
MSV3d	rs137854671
GWAS Ctlg	rs137854671

Max Magnitude

0

ClinVar
Risk	rs137854671(G;G) rs137854671(T;T)
Alt	rs137854671(G;G) rs137854671(T;T)
Reference	Rs137854671(C;C)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31324616G>A; NC_000006.11:g.31324616G>C
CLNSRC
CLNACC