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rs886037621

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886037621(G;T)
Make rs886037621(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome8
Position11564613
GeneBLK
is asnp
is mentioned by
dbSNPrs886037621
dbSNP (classic)rs886037621
ClinGenrs886037621
ebirs886037621
HLIrs886037621
Exacrs886037621
Gnomadrs886037621
Varsomers886037621
LitVarrs886037621
Maprs886037621
PheGenIrs886037621
Biobankrs886037621
1000 genomesrs886037621
hgdprs886037621
ensemblrs886037621
geneviewrs886037621
scholarrs886037621
googlers886037621
pharmgkbrs886037621
gwascentralrs886037621
openSNPrs886037621
23andMers886037621
23andMe allrs886037621
SNPshotrs886037621
SNPdbers886037621
MSV3drs886037621
GWAS Ctlgrs886037621
Max Magnitude0
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,