Have questions? Visit https://www.reddit.com/r/SNPedia

rs786202945

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs786202945(AT;AT)
Make rs786202945(AT;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32396918
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202945
ebirs786202945
HLIrs786202945
Exacrs786202945
Varsomers786202945
Maprs786202945
PheGenIrs786202945
hapmaprs786202945
1000 genomesrs786202945
hgdprs786202945
ensemblrs786202945
gopubmedrs786202945
geneviewrs786202945
scholarrs786202945
googlers786202945
pharmgkbrs786202945
gwascentralrs786202945
openSNPrs786202945
23andMers786202945
23andMe allrs786202945
SNP Nexus

SNPshotrs786202945
SNPdbers786202945
MSV3drs786202945
GWAS Ctlgrs786202945
Max Magnitude0
ClinVar
Risk rs786202945(AT;AT)
Alt rs786202945(AT;AT)
Reference rs786202945(TG;TG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32971055_32971056delTGinsAT
CLNSRC
CLNACC RCV000166021.1,