rs876661205

Orientation

plus

Stabilized

plus

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

Make rs876661205(-;-)

Make rs876661205(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47799952

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs876661205
dbSNP (classic)	rs876661205
ClinGen	rs876661205
ebi	rs876661205
HLI	rs876661205
Exac	rs876661205
Gnomad	rs876661205
Varsome	rs876661205
LitVar	rs876661205
Map	rs876661205
PheGenI	rs876661205
Biobank	rs876661205
1000 genomes	rs876661205
hgdp	rs876661205
ensembl	rs876661205
geneview	rs876661205
scholar	rs876661205
google	rs876661205
pharmgkb	rs876661205
gwascentral	rs876661205
openSNP	rs876661205
23andMe	rs876661205
SNPshot	rs876661205
SNPdbe	rs876661205
MSV3d	rs876661205
GWAS Ctlg	rs876661205

Max Magnitude

0

ClinVar
Risk	rs876661205(-;-)
Alt	rs876661205(-;-)
Reference	Rs876661205(C;C)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48027091delC
CLNSRC
CLNACC	RCV000215322.1, RCV000491140.1,