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rs786202500

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202500(C;T)
Make rs786202500(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position214781378
GeneBARD1
is asnp
is mentioned by
dbSNPrs786202500
ebirs786202500
HLIrs786202500
Exacrs786202500
Varsomers786202500
Maprs786202500
PheGenIrs786202500
hapmaprs786202500
1000 genomesrs786202500
hgdprs786202500
ensemblrs786202500
gopubmedrs786202500
geneviewrs786202500
scholarrs786202500
googlers786202500
pharmgkbrs786202500
gwascentralrs786202500
openSNPrs786202500
23andMers786202500
23andMe allrs786202500
SNP Nexus

SNPshotrs786202500
SNPdbers786202500
MSV3drs786202500
GWAS Ctlgrs786202500
Max Magnitude0
ClinVar
Risk rs786202500(T;T)
Alt rs786202500(T;T)
Reference rs786202500(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BARD1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.215646102G>A
CLNSRC
CLNACC RCV000165343.1,