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rs777937955

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777937955(G;T)
Make rs777937955(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position214752502
GeneBARD1
is asnp
is mentioned by
dbSNPrs777937955
dbSNP (classic)rs777937955
ClinGenrs777937955
ebirs777937955
HLIrs777937955
Exacrs777937955
Gnomadrs777937955
Varsomers777937955
LitVarrs777937955
Maprs777937955
PheGenIrs777937955
Biobankrs777937955
1000 genomesrs777937955
hgdprs777937955
ensemblrs777937955
geneviewrs777937955
scholarrs777937955
googlers777937955
pharmgkbrs777937955
gwascentralrs777937955
openSNPrs777937955
23andMers777937955
23andMe allrs777937955
SNPshotrs777937955
SNPdbers777937955
MSV3drs777937955
GWAS Ctlgrs777937955
Max Magnitude0
ClinVar
Risk rs777937955(A;A) rs777937955(T;T)
Alt rs777937955(A;A) rs777937955(T;T)
Reference Rs777937955(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene BARD1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.215617226G>T
CLNSRC
CLNACC RCV000438118.1,