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rs17489363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs17489363(A;G)
Make rs17489363(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position214809617
GeneBARD1, LOC101928103
is asnp
is mentioned by
dbSNPrs17489363
dbSNP (old)rs17489363
ClinGenrs17489363
ebirs17489363
HLIrs17489363
Exacrs17489363
Gnomadrs17489363
Varsomers17489363
Maprs17489363
PheGenIrs17489363
Biobankrs17489363
1000 genomesrs17489363
hgdprs17489363
ensemblrs17489363
gopubmedrs17489363
geneviewrs17489363
scholarrs17489363
googlers17489363
pharmgkbrs17489363
gwascentralrs17489363
openSNPrs17489363
23andMers17489363
23andMe allrs17489363
SNP Nexus

SNPshotrs17489363
SNPdbers17489363
MSV3drs17489363
GWAS Ctlgrs17489363
GMAF0.2268
Max Magnitude0

[PMID 23056176OA-icon.png] Identification of Functional SNPs in BARD1 Gene and In Silico Analysis of Damaging SNPs: Based on Data Procured from dbSNP Database

ClinVar
Risk rs17489363(G;G)
Alt rs17489363(G;G)
Reference Rs17489363(A;A)
Significance Probable-non-pathogenic
Disease Neoplasm of breast
Variation info
Gene LOC101928103 BARD1
CLNDBN Neoplasm of breast
Reversed 0
HGVS NC_000002.11:g.215674341A>G
CLNSRC
CLNACC RCV000374186.1,