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rs138682654

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138682654(A;A)
Make rs138682654(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6291367
GeneWFS1
is asnp
is mentioned by
dbSNPrs138682654
ebirs138682654
HLIrs138682654
Exacrs138682654
Varsomers138682654
Maprs138682654
PheGenIrs138682654
hapmaprs138682654
1000 genomesrs138682654
hgdprs138682654
ensemblrs138682654
gopubmedrs138682654
geneviewrs138682654
scholarrs138682654
googlers138682654
pharmgkbrs138682654
gwascentralrs138682654
openSNPrs138682654
23andMers138682654
23andMe allrs138682654
SNP Nexus

SNPshotrs138682654
SNPdbers138682654
MSV3drs138682654
GWAS Ctlgrs138682654
Max Magnitude0
ClinVar
Risk rs138682654(A;A)
Alt rs138682654(A;A)
Reference rs138682654(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6293094G>A
CLNSRC
CLNACC RCV000196477.1,