rs876658604

Orientation

plus

Stabilized

plus

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

Make rs876658604(-;-)

Make rs876658604(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47799881

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs876658604
dbSNP (classic)	rs876658604
ClinGen	rs876658604
ebi	rs876658604
HLI	rs876658604
Exac	rs876658604
Gnomad	rs876658604
Varsome	rs876658604
LitVar	rs876658604
Map	rs876658604
PheGenI	rs876658604
Biobank	rs876658604
1000 genomes	rs876658604
hgdp	rs876658604
ensembl	rs876658604
geneview	rs876658604
scholar	rs876658604
google	rs876658604
pharmgkb	rs876658604
gwascentral	rs876658604
openSNP	rs876658604
23andMe	rs876658604
SNPshot	rs876658604
SNPdbe	rs876658604
MSV3d	rs876658604
GWAS Ctlg	rs876658604

Max Magnitude

0

ClinVar
Risk	rs876658604(-;-)
Alt	rs876658604(-;-)
Reference	Rs876658604(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48027020delC
CLNSRC
CLNACC	RCV000221157.2,