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rs786203318

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs786203318(-;-)
Make rs786203318(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32394784
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203318
ebirs786203318
HLIrs786203318
Exacrs786203318
Varsomers786203318
Maprs786203318
PheGenIrs786203318
hapmaprs786203318
1000 genomesrs786203318
hgdprs786203318
ensemblrs786203318
gopubmedrs786203318
geneviewrs786203318
scholarrs786203318
googlers786203318
pharmgkbrs786203318
gwascentralrs786203318
openSNPrs786203318
23andMers786203318
23andMe allrs786203318
SNP Nexus

SNPshotrs786203318
SNPdbers786203318
MSV3drs786203318
GWAS Ctlgrs786203318
Max Magnitude0
ClinVar
Risk rs786203318(;)
Alt rs786203318(;)
Reference rs786203318(AT;AT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32968921_32968922delAT
CLNSRC
CLNACC RCV000166577.1,