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rs61757642

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61757642(A;T)
Make rs61757642(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394936
GeneBRCA2
is asnp
is mentioned by
dbSNPrs61757642
ebirs61757642
HLIrs61757642
Exacrs61757642
Varsomers61757642
Maprs61757642
PheGenIrs61757642
hapmaprs61757642
1000 genomesrs61757642
hgdprs61757642
ensemblrs61757642
gopubmedrs61757642
geneviewrs61757642
scholarrs61757642
googlers61757642
pharmgkbrs61757642
gwascentralrs61757642
openSNPrs61757642
23andMers61757642
23andMe allrs61757642
SNP Nexus

SNPshotrs61757642
SNPdbers61757642
MSV3drs61757642
GWAS Ctlgrs61757642
Max Magnitude0
ClinVar
Risk rs61757642(T;T)
Alt rs61757642(T;T)
Reference rs61757642(A;A)
Significance Other
Disease Breast-ovarian cancer not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32969073A>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031825.7, RCV000045838.6, RCV000131261.2, RCV000167798.4,