Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880423

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880423(A;T)
Make rs730880423(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position8745860
GeneCAV3, SSUH2
is asnp
is mentioned by
dbSNPrs730880423
ebirs730880423
HLIrs730880423
Exacrs730880423
Varsomers730880423
Maprs730880423
PheGenIrs730880423
hapmaprs730880423
1000 genomesrs730880423
hgdprs730880423
ensemblrs730880423
gopubmedrs730880423
geneviewrs730880423
scholarrs730880423
googlers730880423
pharmgkbrs730880423
gwascentralrs730880423
openSNPrs730880423
23andMers730880423
23andMe allrs730880423
SNP Nexus

SNPshotrs730880423
SNPdbers730880423
MSV3drs730880423
GWAS Ctlgrs730880423
Max Magnitude0
ClinVar
Risk rs730880423(T;T)
Alt rs730880423(T;T)
Reference rs730880423(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene SSUH2 CAV3
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.8787546A>T
CLNSRC
CLNACC RCV000157843.2,