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rs786202791

From SNPedia

Orientationminus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs786202791(-;-)
Make rs786202791(-;TA)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43092207
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786202791
ebirs786202791
HLIrs786202791
Exacrs786202791
Varsomers786202791
Maprs786202791
PheGenIrs786202791
hapmaprs786202791
1000 genomesrs786202791
hgdprs786202791
ensemblrs786202791
gopubmedrs786202791
geneviewrs786202791
scholarrs786202791
googlers786202791
pharmgkbrs786202791
gwascentralrs786202791
openSNPrs786202791
23andMers786202791
23andMe allrs786202791
SNP Nexus

SNPshotrs786202791
SNPdbers786202791
MSV3drs786202791
GWAS Ctlgrs786202791
Max Magnitude0
ClinVar
Risk rs786202791(;)
Alt rs786202791(;)
Reference rs786202791(TA;TA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41244224_41244225delTA
CLNSRC
CLNACC RCV000165779.1,