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rs786203694

From SNPedia

Orientationminus
Geno Mag Summary
(AAGGAAGATA;AAGGAAGATA) 0 common in clinvar
Make rs786203694(-;-)
Make rs786203694(-;AAGGAAGATA)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43092044
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786203694
ebirs786203694
HLIrs786203694
Exacrs786203694
Varsomers786203694
Maprs786203694
PheGenIrs786203694
hapmaprs786203694
1000 genomesrs786203694
hgdprs786203694
ensemblrs786203694
gopubmedrs786203694
geneviewrs786203694
scholarrs786203694
googlers786203694
pharmgkbrs786203694
gwascentralrs786203694
openSNPrs786203694
23andMers786203694
23andMe allrs786203694
SNP Nexus

SNPshotrs786203694
SNPdbers786203694
MSV3drs786203694
GWAS Ctlgrs786203694
Max Magnitude0
ClinVar
Risk rs786203694(;)
Alt rs786203694(;)
Reference rs786203694(AAGGAAGATA;AAGGAAGATA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41244061_41244070delTATCTTCCTT
CLNSRC
CLNACC RCV000167110.1,