rs45509993

Orientation

minus

Stabilized

minus

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

Make rs45509993(A;A)

Make rs45509993(A;C)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31356898

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs45509993
dbSNP (classic)	rs45509993
ClinGen	rs45509993
ebi	rs45509993
HLI	rs45509993
Exac	rs45509993
Gnomad	rs45509993
Varsome	rs45509993
LitVar	rs45509993
Map	rs45509993
PheGenI	rs45509993
Biobank	rs45509993
1000 genomes	rs45509993
hgdp	rs45509993
ensembl	rs45509993
geneview	rs45509993
scholar	rs45509993
google	rs45509993
pharmgkb	rs45509993
gwascentral	rs45509993
openSNP	rs45509993
23andMe	rs45509993
SNPshot	rs45509993
SNPdbe	rs45509993
MSV3d	rs45509993
GWAS Ctlg	rs45509993

Max Magnitude

0

ClinVar
Risk	rs45509993(A;A) rs45509993(G;G) rs45509993(T;T)
Alt	rs45509993(A;A) rs45509993(G;G) rs45509993(T;T)
Reference	Rs45509993(C;C)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31324675G>A; NC_000006.11:g.31324675G>C; NC_000006.11:g.31324675G>T
CLNSRC
CLNACC