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rs200095753

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200095753(C;T)
Make rs200095753(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6300918
GeneWFS1
is asnp
is mentioned by
dbSNPrs200095753
ebirs200095753
HLIrs200095753
Exacrs200095753
Varsomers200095753
Maprs200095753
PheGenIrs200095753
hapmaprs200095753
1000 genomesrs200095753
hgdprs200095753
ensemblrs200095753
gopubmedrs200095753
geneviewrs200095753
scholarrs200095753
googlers200095753
pharmgkbrs200095753
gwascentralrs200095753
openSNPrs200095753
23andMers200095753
23andMe allrs200095753
SNP Nexus

SNPshotrs200095753
SNPdbers200095753
MSV3drs200095753
GWAS Ctlgrs200095753
Max Magnitude0
ClinVar
Risk rs200095753(A,T;A,T)
Alt rs200095753(A,T;A,T)
Reference rs200095753(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6302645C>T
CLNSRC
CLNACC RCV000196031.1,