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rs786203149

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203149(-;-)
Make rs786203149(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43076593
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786203149
ebirs786203149
HLIrs786203149
Exacrs786203149
Varsomers786203149
Maprs786203149
PheGenIrs786203149
hapmaprs786203149
1000 genomesrs786203149
hgdprs786203149
ensemblrs786203149
gopubmedrs786203149
geneviewrs786203149
scholarrs786203149
googlers786203149
pharmgkbrs786203149
gwascentralrs786203149
openSNPrs786203149
23andMers786203149
23andMe allrs786203149
SNP Nexus

SNPshotrs786203149
SNPdbers786203149
MSV3drs786203149
GWAS Ctlgrs786203149
Max Magnitude0
ClinVar
Risk rs786203149(;)
Alt rs786203149(;)
Reference rs786203149(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.41228610delC
CLNSRC
CLNACC RCV000166328.1,