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rs786203438

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203438(G;T)
Make rs786203438(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43092050
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786203438
ebirs786203438
HLIrs786203438
Exacrs786203438
Varsomers786203438
Maprs786203438
PheGenIrs786203438
hapmaprs786203438
1000 genomesrs786203438
hgdprs786203438
ensemblrs786203438
gopubmedrs786203438
geneviewrs786203438
scholarrs786203438
googlers786203438
pharmgkbrs786203438
gwascentralrs786203438
openSNPrs786203438
23andMers786203438
23andMe allrs786203438
SNP Nexus

SNPshotrs786203438
SNPdbers786203438
MSV3drs786203438
GWAS Ctlgrs786203438
Max Magnitude0
ClinVar
Risk rs786203438(T;T)
Alt rs786203438(T;T)
Reference rs786203438(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41244067C>A
CLNSRC
CLNACC RCV000166742.1,