Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508048

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs397508048(G;G)
Make rs397508048(G;TA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394788
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508048
ebirs397508048
HLIrs397508048
Exacrs397508048
Varsomers397508048
Maprs397508048
PheGenIrs397508048
hapmaprs397508048
1000 genomesrs397508048
hgdprs397508048
ensemblrs397508048
gopubmedrs397508048
geneviewrs397508048
scholarrs397508048
googlers397508048
pharmgkbrs397508048
gwascentralrs397508048
openSNPrs397508048
23andMers397508048
23andMe allrs397508048
SNP Nexus

SNPshotrs397508048
SNPdbers397508048
MSV3drs397508048
GWAS Ctlgrs397508048
Max Magnitude0
ClinVar
Risk rs397508048(G;G)
Alt rs397508048(G;G)
Reference rs397508048(TA;TA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32968925_32968926delTAinsG
CLNSRC ClinVar
CLNACC RCV000045799.2,