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rs1064794741

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome18
Position11881049
GeneGNAL
is asnp
is mentioned by
dbSNPrs1064794741
dbSNP (old)rs1064794741
ClinGenrs1064794741
ebirs1064794741
HLIrs1064794741
Exacrs1064794741
Gnomadrs1064794741
Varsomers1064794741
Maprs1064794741
PheGenIrs1064794741
Biobankrs1064794741
1000 genomesrs1064794741
hgdprs1064794741
ensemblrs1064794741
gopubmedrs1064794741
geneviewrs1064794741
scholarrs1064794741
googlers1064794741
pharmgkbrs1064794741
gwascentralrs1064794741
openSNPrs1064794741
23andMers1064794741
23andMe allrs1064794741
SNPshotrs1064794741
SNPdbers1064794741
MSV3drs1064794741
GWAS Ctlgrs1064794741
Max Magnitude0
ClinVar
Risk rs1064794741(A;A)
Alt rs1064794741(A;A)
Reference Rs1064794741(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GNAL
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.11881048G>A
CLNSRC
CLNACC RCV000484326.1,