rs137854759

Orientation

minus

Stabilized

minus

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

Make rs137854759(C;C)

Make rs137854759(C;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31356249

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs137854759
dbSNP (classic)	rs137854759
ClinGen	rs137854759
ebi	rs137854759
HLI	rs137854759
Exac	rs137854759
Gnomad	rs137854759
Varsome	rs137854759
LitVar	rs137854759
Map	rs137854759
PheGenI	rs137854759
Biobank	rs137854759
1000 genomes	rs137854759
hgdp	rs137854759
ensembl	rs137854759
geneview	rs137854759
scholar	rs137854759
google	rs137854759
pharmgkb	rs137854759
gwascentral	rs137854759
openSNP	rs137854759
23andMe	rs137854759
SNPshot	rs137854759
SNPdbe	rs137854759
MSV3d	rs137854759
GWAS Ctlg	rs137854759

Max Magnitude

0

ClinVar
Risk	rs137854759(A;A) rs137854759(C;C)
Alt	rs137854759(A;A) rs137854759(C;C)
Reference	Rs137854759(G;G)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31324026C>G; NC_000006.11:g.31324026C>T
CLNSRC
CLNACC