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rs797045076

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTTC;TTTC) 0 common in clinvar
Make rs797045076(-;-)
Make rs797045076(-;TCTT)
Make rs797045076(TCTT;TCTT)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6302443
GeneWFS1
is asnp
is mentioned by
dbSNPrs797045076
ClinGenrs797045076
ebirs797045076
HLIrs797045076
Exacrs797045076
Varsomers797045076
Maprs797045076
PheGenIrs797045076
hapmaprs797045076
1000 genomesrs797045076
hgdprs797045076
ensemblrs797045076
gopubmedrs797045076
geneviewrs797045076
scholarrs797045076
googlers797045076
pharmgkbrs797045076
gwascentralrs797045076
openSNPrs797045076
23andMers797045076
23andMe allrs797045076
SNP Nexus

SNPshotrs797045076
SNPdbers797045076
MSV3drs797045076
GWAS Ctlgrs797045076
Max Magnitude0
ClinVar
Risk rs797045076(-;-) Rs797045076(TTTC;TTTC)
Alt rs797045076(-;-) Rs797045076(TTTC;TTTC)
Reference rs797045076(TCTT;TCTT)
Significance Pathogenic
Disease Diabetes mellitus AND insipidus with optic atrophy AND deafness not provided
Variation info
Gene WFS1
CLNDBN Diabetes mellitus AND insipidus with optic atrophy AND deafness not provided
Reversed 0
HGVS NC_000004.11:g.6304170_6304173delTCTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000191146.2, RCV000200365.1,