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rs730880420

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880420(C;C)
Make rs730880420(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position8745662
GeneCAV3, SSUH2
is asnp
is mentioned by
dbSNPrs730880420
ebirs730880420
HLIrs730880420
Exacrs730880420
Varsomers730880420
Maprs730880420
PheGenIrs730880420
hapmaprs730880420
1000 genomesrs730880420
hgdprs730880420
ensemblrs730880420
gopubmedrs730880420
geneviewrs730880420
scholarrs730880420
googlers730880420
pharmgkbrs730880420
gwascentralrs730880420
openSNPrs730880420
23andMers730880420
23andMe allrs730880420
SNP Nexus

SNPshotrs730880420
SNPdbers730880420
MSV3drs730880420
GWAS Ctlgrs730880420
Max Magnitude0
ClinVar
Risk rs730880420(C;C)
Alt rs730880420(C;C)
Reference rs730880420(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SSUH2 CAV3
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.8787348T>C
CLNSRC
CLNACC RCV000157836.1,