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rs786203663

From SNPedia

Orientationminus
Geno Mag Summary
(TGTGG;TGTGG) 0 common in clinvar
Make rs786203663(AGTGA;AGTGA)
Make rs786203663(AGTGA;TGTGG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43049164
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786203663
ebirs786203663
HLIrs786203663
Exacrs786203663
Varsomers786203663
Maprs786203663
PheGenIrs786203663
hapmaprs786203663
1000 genomesrs786203663
hgdprs786203663
ensemblrs786203663
gopubmedrs786203663
geneviewrs786203663
scholarrs786203663
googlers786203663
pharmgkbrs786203663
gwascentralrs786203663
openSNPrs786203663
23andMers786203663
23andMe allrs786203663
SNP Nexus

SNPshotrs786203663
SNPdbers786203663
MSV3drs786203663
GWAS Ctlgrs786203663
Max Magnitude0
ClinVar
Risk rs786203663(AGTGA;AGTGA)
Alt rs786203663(AGTGA;AGTGA)
Reference rs786203663(TGTGG;TGTGG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41201181_41201185delCCACAinsTCACT
CLNSRC
CLNACC RCV000167071.1, RCV000239024.1,