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rs794726687

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794726687(-;-)
Make rs794726687(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position108898939
GeneGPSM2
is asnp
is mentioned by
dbSNPrs794726687
ebirs794726687
HLIrs794726687
Exacrs794726687
Varsomers794726687
Maprs794726687
PheGenIrs794726687
hapmaprs794726687
1000 genomesrs794726687
hgdprs794726687
ensemblrs794726687
gopubmedrs794726687
geneviewrs794726687
scholarrs794726687
googlers794726687
pharmgkbrs794726687
gwascentralrs794726687
openSNPrs794726687
23andMers794726687
23andMe allrs794726687
SNP Nexus

SNPshotrs794726687
SNPdbers794726687
MSV3drs794726687
GWAS Ctlgrs794726687
Max Magnitude0
ClinVar
Risk rs794726687(;)
Alt rs794726687(;)
Reference rs794726687(C;C)
Significance Pathogenic
Disease Chudley-McCullough syndrome not provided
Variation info
Gene GPSM2
CLNDBN Chudley-McCullough syndrome not provided
Reversed 0
HGVS NC_000001.10:g.109441561delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000029164.4, RCV000223985.1,