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rs761283105

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761283105(C;T)
Make rs761283105(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position74747731
GeneGFM2
is asnp
is mentioned by
dbSNPrs761283105
ebirs761283105
HLIrs761283105
Exacrs761283105
Varsomers761283105
Maprs761283105
PheGenIrs761283105
hapmaprs761283105
1000 genomesrs761283105
hgdprs761283105
ensemblrs761283105
gopubmedrs761283105
geneviewrs761283105
scholarrs761283105
googlers761283105
pharmgkbrs761283105
gwascentralrs761283105
openSNPrs761283105
23andMers761283105
23andMe allrs761283105
SNP Nexus

SNPshotrs761283105
SNPdbers761283105
MSV3drs761283105
GWAS Ctlgrs761283105
Max Magnitude0
ClinVar
Risk rs761283105(T;T)
Alt rs761283105(T;T)
Reference rs761283105(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GFM2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.74043556C>T
CLNSRC
CLNACC RCV000197518.1,