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

rs139785364

From SNPedia

Orientationplus
Stabilizedplus
Make rs139785364(A;A)
Make rs139785364(A;G)
Make rs139785364(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position214728759
GeneBARD1
is asnp
is mentioned by
dbSNPrs139785364
dbSNP (old)rs139785364
ClinGenrs139785364
ebirs139785364
HLIrs139785364
Exacrs139785364
Gnomadrs139785364
Varsomers139785364
Maprs139785364
PheGenIrs139785364
Biobankrs139785364
1000 genomesrs139785364
hgdprs139785364
ensemblrs139785364
gopubmedrs139785364
geneviewrs139785364
scholarrs139785364
googlers139785364
pharmgkbrs139785364
gwascentralrs139785364
openSNPrs139785364
23andMers139785364
23andMe allrs139785364
SNP Nexus

SNPshotrs139785364
SNPdbers139785364
MSV3drs139785364
GWAS Ctlgrs139785364
Max Magnitude

[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 rs139785364(A;A)
Alt rs139785364(A;A)
Reference rs139785364(G;G)
Significance Unknown
Disease not specified
Variation info
Gene BARD1
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.215593483G>A
CLNSRC
CLNACC RCV000484312.1,