rs886037621

Orientation

plus

Stabilized

plus

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

Make rs886037621(G;T)

Make rs886037621(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

8

Position

11564613

Gene

BLK

is a	snp
is	mentioned by
dbSNP	rs886037621
dbSNP (classic)	rs886037621
ClinGen	rs886037621
ebi	rs886037621
HLI	rs886037621
Exac	rs886037621
Gnomad	rs886037621
Varsome	rs886037621
LitVar	rs886037621
Map	rs886037621
PheGenI	rs886037621
Biobank	rs886037621
1000 genomes	rs886037621
hgdp	rs886037621
ensembl	rs886037621
geneview	rs886037621
scholar	rs886037621
google	rs886037621
pharmgkb	rs886037621
gwascentral	rs886037621
openSNP	rs886037621
23andMe	rs886037621
SNPshot	rs886037621
SNPdbe	rs886037621
MSV3d	rs886037621
GWAS Ctlg	rs886037621

Max Magnitude

0

ClinVar
Risk	rs886037621(T;T)
Alt	rs886037621(T;T)
Reference	Rs886037621(G;G)
Significance	Pathogenic
Disease	Maturity-onset diabetes of the young
Variation	info
Gene	BLK
CLNDBN	Maturity-onset diabetes of the young, type 11
Reversed	0
HGVS	NC_000008.10:g.11422122G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013116.22,