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rs397509168

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCTT;CCTT) 0 common in clinvar
Make rs397509168(-;-)
Make rs397509168(-;CCTT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43104123
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509168
ebirs397509168
HLIrs397509168
Exacrs397509168
Varsomers397509168
Maprs397509168
PheGenIrs397509168
hapmaprs397509168
1000 genomesrs397509168
hgdprs397509168
ensemblrs397509168
gopubmedrs397509168
geneviewrs397509168
scholarrs397509168
googlers397509168
pharmgkbrs397509168
gwascentralrs397509168
openSNPrs397509168
23andMers397509168
23andMe allrs397509168
SNP Nexus

SNPshotrs397509168
SNPdbers397509168
MSV3drs397509168
GWAS Ctlgrs397509168
Max Magnitude0
ClinVar
Risk rs397509168(;)
Alt rs397509168(;)
Reference rs397509168(CCTT;CCTT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41256140_41256143delAAGG
CLNSRC ClinVar
CLNACC RCV000048543.2,