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rs587781527

From SNPedia

Orientationminus
Geno Mag Summary
(GGAGGTC;GGAGGTC) 0 common in clinvar
Make rs587781527(GGAGGTC;TGAGGTT)
Make rs587781527(TGAGGTT;TGAGGTT)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position35103466
GeneRAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs587781527
ebirs587781527
HLIrs587781527
Exacrs587781527
Varsomers587781527
Maprs587781527
PheGenIrs587781527
hapmaprs587781527
1000 genomesrs587781527
hgdprs587781527
ensemblrs587781527
gopubmedrs587781527
geneviewrs587781527
scholarrs587781527
googlers587781527
pharmgkbrs587781527
gwascentralrs587781527
openSNPrs587781527
23andMers587781527
23andMe allrs587781527
SNP Nexus

SNPshotrs587781527
SNPdbers587781527
MSV3drs587781527
GWAS Ctlgrs587781527
Max Magnitude0
ClinVar
Risk rs587781527(TGAGGTT;TGAGGTT)
Alt rs587781527(TGAGGTT;TGAGGTT)
Reference rs587781527(GGAGGTC;GGAGGTC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51D RAD51L3-RFFL
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.33430485_33430491delGACCTCCinsAACCTCA
CLNSRC
CLNACC RCV000129520.1,