rs786202500

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs786202500(C;T)

Make rs786202500(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

214781378

Gene

BARD1

is a	snp
is	mentioned by
dbSNP	rs786202500
dbSNP (classic)	rs786202500
ClinGen	rs786202500
ebi	rs786202500
HLI	rs786202500
Exac	rs786202500
Gnomad	rs786202500
Varsome	rs786202500
LitVar	rs786202500
Map	rs786202500
PheGenI	rs786202500
Biobank	rs786202500
1000 genomes	rs786202500
hgdp	rs786202500
ensembl	rs786202500
geneview	rs786202500
scholar	rs786202500
google	rs786202500
pharmgkb	rs786202500
gwascentral	rs786202500
openSNP	rs786202500
23andMe	rs786202500
SNPshot	rs786202500
SNPdbe	rs786202500
MSV3d	rs786202500
GWAS Ctlg	rs786202500

Max Magnitude

0

ClinVar
Risk	rs786202500(T;T)
Alt	rs786202500(T;T)
Reference	Rs786202500(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BARD1
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000002.11:g.215646102G>A
CLNSRC
CLNACC	RCV000165343.2, RCV000437177.1,