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rs200672755

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200672755(A;A)
Make rs200672755(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6301815
GeneWFS1
is asnp
is mentioned by
dbSNPrs200672755
ebirs200672755
HLIrs200672755
Exacrs200672755
Varsomers200672755
Maprs200672755
PheGenIrs200672755
hapmaprs200672755
1000 genomesrs200672755
hgdprs200672755
ensemblrs200672755
gopubmedrs200672755
geneviewrs200672755
scholarrs200672755
googlers200672755
pharmgkbrs200672755
gwascentralrs200672755
openSNPrs200672755
23andMers200672755
23andMe allrs200672755
SNP Nexus

SNPshotrs200672755
SNPdbers200672755
MSV3drs200672755
GWAS Ctlgrs200672755
Max Magnitude0
ClinVar
Risk rs200672755(A,C;A,C)
Alt rs200672755(A,C;A,C)
Reference rs200672755(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6303542G>A
CLNSRC
CLNACC RCV000197395.1,