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

rs730882119

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730882119(-;-)
Make rs730882119(-;C)
Make rs730882119(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position35107384
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs730882119
ebirs730882119
HLIrs730882119
Exacrs730882119
Varsomers730882119
Maprs730882119
PheGenIrs730882119
hapmaprs730882119
1000 genomesrs730882119
hgdprs730882119
ensemblrs730882119
gopubmedrs730882119
geneviewrs730882119
scholarrs730882119
googlers730882119
pharmgkbrs730882119
gwascentralrs730882119
openSNPrs730882119
23andMers730882119
23andMe allrs730882119
SNP Nexus

SNPshotrs730882119
SNPdbers730882119
MSV3drs730882119
GWAS Ctlgrs730882119
Max Magnitude0
ClinVar
Risk rs730882119(C;C)
Alt rs730882119(C;C)
Reference rs730882119(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 4
Reversed 1
HGVS NC_000017.10:g.33434404dupG
CLNSRC
CLNACC RCV000160938.1, RCV000178184.1,