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rs753237278

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs753237278(A;A)
Make rs753237278(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6301479
GeneWFS1
is asnp
is mentioned by
dbSNPrs753237278
ebirs753237278
HLIrs753237278
Exacrs753237278
Varsomers753237278
Maprs753237278
PheGenIrs753237278
hapmaprs753237278
1000 genomesrs753237278
hgdprs753237278
ensemblrs753237278
gopubmedrs753237278
geneviewrs753237278
scholarrs753237278
googlers753237278
pharmgkbrs753237278
gwascentralrs753237278
openSNPrs753237278
23andMers753237278
23andMe allrs753237278
SNP Nexus

SNPshotrs753237278
SNPdbers753237278
MSV3drs753237278
GWAS Ctlgrs753237278
Max Magnitude0
ClinVar
Risk rs753237278(A;A)
Alt rs753237278(A;A)
Reference rs753237278(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6303206G>C
CLNSRC
CLNACC RCV000198315.2,