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rs750621215

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs750621215(A;A)
Make rs750621215(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position35101206
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs750621215
ebirs750621215
HLIrs750621215
Exacrs750621215
Varsomers750621215
Maprs750621215
PheGenIrs750621215
hapmaprs750621215
1000 genomesrs750621215
hgdprs750621215
ensemblrs750621215
gopubmedrs750621215
geneviewrs750621215
scholarrs750621215
googlers750621215
pharmgkbrs750621215
gwascentralrs750621215
openSNPrs750621215
23andMers750621215
23andMe allrs750621215
SNP Nexus

SNPshotrs750621215
SNPdbers750621215
MSV3drs750621215
GWAS Ctlgrs750621215
Max Magnitude0
ClinVar
Risk rs750621215(A;A)
Alt rs750621215(A;A)
Reference rs750621215(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer not provided
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 4 not provided
Reversed 0
HGVS NC_000017.10:g.33428225G>A
CLNSRC
CLNACC RCV000164406.1, RCV000227954.1, RCV000235877.1,