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rs730882134

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730882134(-;-)
Make rs730882134(-;TA)
Make rs730882134(TA;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32337702
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730882134
ebirs730882134
HLIrs730882134
Exacrs730882134
Varsomers730882134
Maprs730882134
PheGenIrs730882134
hapmaprs730882134
1000 genomesrs730882134
hgdprs730882134
ensemblrs730882134
gopubmedrs730882134
geneviewrs730882134
scholarrs730882134
googlers730882134
pharmgkbrs730882134
gwascentralrs730882134
openSNPrs730882134
23andMers730882134
23andMe allrs730882134
SNP Nexus

SNPshotrs730882134
SNPdbers730882134
MSV3drs730882134
GWAS Ctlgrs730882134
Max Magnitude0
ClinVar
Risk rs730882134(TA;TA)
Alt rs730882134(TA;TA)
Reference rs730882134(;)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32911839_32911840insTA
CLNSRC
CLNACC RCV000161943.1,