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rs786202157

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786202157(-;-)
Make rs786202157(-;AAAG)
Make rs786202157(AAAG;AAAG)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32341018
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202157
ebirs786202157
HLIrs786202157
Exacrs786202157
Varsomers786202157
Maprs786202157
PheGenIrs786202157
hapmaprs786202157
1000 genomesrs786202157
hgdprs786202157
ensemblrs786202157
gopubmedrs786202157
geneviewrs786202157
scholarrs786202157
googlers786202157
pharmgkbrs786202157
gwascentralrs786202157
openSNPrs786202157
23andMers786202157
23andMe allrs786202157
SNP Nexus

SNPshotrs786202157
SNPdbers786202157
MSV3drs786202157
GWAS Ctlgrs786202157
Max Magnitude0
ClinVar
Risk rs786202157(AAAG;AAAG)
Alt rs786202157(AAAG;AAAG)
Reference rs786202157(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32915155_32915156insAAAG
CLNSRC
CLNACC RCV000164833.1,