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rs397507851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAATGTT;AAATGTT) 0 common in clinvar
(TTAAATG;TTAAATG) 0 common in clinvar
Make rs397507851(-;-)
Make rs397507851(-;AAATGTT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340763
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507851
ebirs397507851
HLIrs397507851
Exacrs397507851
Varsomers397507851
Maprs397507851
PheGenIrs397507851
hapmaprs397507851
1000 genomesrs397507851
hgdprs397507851
ensemblrs397507851
gopubmedrs397507851
geneviewrs397507851
scholarrs397507851
googlers397507851
pharmgkbrs397507851
gwascentralrs397507851
openSNPrs397507851
23andMers397507851
23andMe allrs397507851
SNP Nexus

SNPshotrs397507851
SNPdbers397507851
MSV3drs397507851
GWAS Ctlgrs397507851
Max Magnitude0
ClinVar
Risk rs397507851(;)
Alt rs397507851(;)
Reference rs397507851(TTAAATG;TTAAATG)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32914900_32914906delAAATGTT
CLNSRC ClinVar
CLNACC RCV000044937.2, RCV000166653.1,