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rs1060502318

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs1060502318(-;-)
Make rs1060502318(-;GG)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position8733882
GeneCAV3, SSUH2
is asnp
is mentioned by
dbSNPrs1060502318
dbSNP (old)rs1060502318
ClinGenrs1060502318
ebirs1060502318
HLIrs1060502318
Exacrs1060502318
Gnomadrs1060502318
Varsomers1060502318
LitVarrs1060502318
Maprs1060502318
PheGenIrs1060502318
Biobankrs1060502318
1000 genomesrs1060502318
hgdprs1060502318
ensemblrs1060502318
gopubmedrs1060502318
geneviewrs1060502318
scholarrs1060502318
googlers1060502318
pharmgkbrs1060502318
gwascentralrs1060502318
openSNPrs1060502318
23andMers1060502318
23andMe allrs1060502318
SNPshotrs1060502318
SNPdbers1060502318
MSV3drs1060502318
GWAS Ctlgrs1060502318
Max Magnitude0
ClinVar
Risk rs1060502318(-;-)
Alt rs1060502318(-;-)
Reference Rs1060502318(GG;GG)
Significance Pathogenic
Disease Long QT syndrome
Variation info
Gene SSUH2 CAV3
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000003.11:g.8775568_8775569delGG
CLNSRC
CLNACC RCV000464773.1,