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rs770828281

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770828281(C;T)
Make rs770828281(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position75980923
GeneTGFB3
is asnp
is mentioned by
dbSNPrs770828281
ebirs770828281
HLIrs770828281
Exacrs770828281
Varsomers770828281
Maprs770828281
PheGenIrs770828281
hapmaprs770828281
1000 genomesrs770828281
hgdprs770828281
ensemblrs770828281
gopubmedrs770828281
geneviewrs770828281
scholarrs770828281
googlers770828281
pharmgkbrs770828281
gwascentralrs770828281
openSNPrs770828281
23andMers770828281
23andMe allrs770828281
SNP Nexus

SNPshotrs770828281
SNPdbers770828281
MSV3drs770828281
GWAS Ctlgrs770828281
Max Magnitude0
ClinVar
Risk rs770828281(T;T)
Alt rs770828281(T;T)
Reference rs770828281(C;C)
Significance Pathogenic
Disease Arrhythmogenic right ventricular dysplasia
Variation info
Gene TGFB3
CLNDBN Arrhythmogenic right ventricular dysplasia, familial 1
Reversed 0
HGVS NC_000014.8:g.76447266C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013292.24,