rs786202646

Merged into

rs753153576

Orientation

plus

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

Make rs786202646(A;A)

Make rs786202646(A;C)

Make rs786202646(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

23626235

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs786202646
dbSNP (classic)	rs786202646
ClinGen	rs786202646
ebi	rs786202646
HLI	rs786202646
Exac	rs786202646
Gnomad	rs786202646
Varsome	rs786202646
LitVar	rs786202646
Map	rs786202646
PheGenI	rs786202646
Biobank	rs786202646
1000 genomes	rs786202646
hgdp	rs786202646
ensembl	rs786202646
geneview	rs786202646
scholar	rs786202646
google	rs786202646
pharmgkb	rs786202646
gwascentral	rs786202646
openSNP	rs786202646
23andMe	rs786202646
SNPshot	rs786202646
SNPdbe	rs786202646
MSV3d	rs786202646
GWAS Ctlg	rs786202646

Status

Merged into rs753153576

Max Magnitude

0

ClinVar
Risk	rs786202646(T;T)
Alt	rs786202646(T;T)
Reference	Rs786202646(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.10:g.23626235C>A
CLNSRC
CLNACC	RCV000165555.1,