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rs397508830

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAAACTGCCA;GAAACTGCCA) 0 common in clinvar
Make rs397508830(-;-)
Make rs397508830(-;GAAACTGCCA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094454
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508830
ebirs397508830
HLIrs397508830
Exacrs397508830
Varsomers397508830
Maprs397508830
PheGenIrs397508830
hapmaprs397508830
1000 genomesrs397508830
hgdprs397508830
ensemblrs397508830
gopubmedrs397508830
geneviewrs397508830
scholarrs397508830
googlers397508830
pharmgkbrs397508830
gwascentralrs397508830
openSNPrs397508830
23andMers397508830
23andMe allrs397508830
SNP Nexus

SNPshotrs397508830
SNPdbers397508830
MSV3drs397508830
GWAS Ctlgrs397508830
Max Magnitude0
ClinVar
Risk rs397508830(;)
Alt rs397508830(;)
Reference rs397508830(GAAACTGCCA;GAAACTGCCA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246471_41246480delTGGCAGTTTC
CLNSRC ClinVar
CLNACC RCV000047328.2,