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rs199910987

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199910987(A;A)
Make rs199910987(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6301405
GeneWFS1
is asnp
is mentioned by
dbSNPrs199910987
ebirs199910987
HLIrs199910987
Exacrs199910987
Varsomers199910987
Maprs199910987
PheGenIrs199910987
hapmaprs199910987
1000 genomesrs199910987
hgdprs199910987
ensemblrs199910987
gopubmedrs199910987
geneviewrs199910987
scholarrs199910987
googlers199910987
pharmgkbrs199910987
gwascentralrs199910987
openSNPrs199910987
23andMers199910987
23andMe allrs199910987
SNP Nexus

SNPshotrs199910987
SNPdbers199910987
MSV3drs199910987
GWAS Ctlgrs199910987
Max Magnitude0
ClinVar
Risk rs199910987(A;A)
Alt rs199910987(A;A)
Reference rs199910987(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6303132G>A
CLNSRC
CLNACC RCV000200051.2,