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rs876657735

From SNPedia

Orientationplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs876657735(-;-)
Make rs876657735(-;TTC)
Make rs876657735(TTC;TTC)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position6300855
GeneWFS1
is asnp
is mentioned by
dbSNPrs876657735
ebirs876657735
HLIrs876657735
Exacrs876657735
Varsomers876657735
Maprs876657735
PheGenIrs876657735
hapmaprs876657735
1000 genomesrs876657735
hgdprs876657735
ensemblrs876657735
gopubmedrs876657735
geneviewrs876657735
scholarrs876657735
googlers876657735
pharmgkbrs876657735
gwascentralrs876657735
openSNPrs876657735
23andMers876657735
23andMe allrs876657735
SNP Nexus

SNPshotrs876657735
SNPdbers876657735
MSV3drs876657735
GWAS Ctlgrs876657735
Max Magnitude0
ClinVar
Risk rs876657735(;)
Alt rs876657735(;)
Reference rs876657735(CTT;CTT)
Significance Pathogenic
Disease Diabetes mellitus AND insipidus with optic atrophy AND deafness
Variation info
Gene WFS1
CLNDBN Diabetes mellitus AND insipidus with optic atrophy AND deafness
Reversed 0
HGVS NC_000004.11:g.6302582_6302584delTTC
CLNSRC
CLNACC RCV000215662.1,