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rs773068151

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773068151(G;T)
Make rs773068151(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position108904124
GeneGPSM2
is asnp
is mentioned by
dbSNPrs773068151
ebirs773068151
HLIrs773068151
Exacrs773068151
Varsomers773068151
Maprs773068151
PheGenIrs773068151
hapmaprs773068151
1000 genomesrs773068151
hgdprs773068151
ensemblrs773068151
gopubmedrs773068151
geneviewrs773068151
scholarrs773068151
googlers773068151
pharmgkbrs773068151
gwascentralrs773068151
openSNPrs773068151
23andMers773068151
23andMe allrs773068151
SNP Nexus

SNPshotrs773068151
SNPdbers773068151
MSV3drs773068151
GWAS Ctlgrs773068151
Max Magnitude0
ClinVar
Risk rs773068151(T;T)
Alt rs773068151(T;T)
Reference rs773068151(G;G)
Significance Pathogenic
Disease Chudley-McCullough syndrome
Variation info
Gene GPSM2
CLNDBN Chudley-McCullough syndrome
Reversed 0
HGVS NC_000001.10:g.109446746G>T
CLNSRC
CLNACC RCV000218080.1,