rs876661033

Orientation

plus

Stabilized

plus

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

Make rs876661033(-;-)

Make rs876661033(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47799628

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs876661033
dbSNP (classic)	rs876661033
ClinGen	rs876661033
ebi	rs876661033
HLI	rs876661033
Exac	rs876661033
Gnomad	rs876661033
Varsome	rs876661033
LitVar	rs876661033
Map	rs876661033
PheGenI	rs876661033
Biobank	rs876661033
1000 genomes	rs876661033
hgdp	rs876661033
ensembl	rs876661033
geneview	rs876661033
scholar	rs876661033
google	rs876661033
pharmgkb	rs876661033
gwascentral	rs876661033
openSNP	rs876661033
23andMe	rs876661033
SNPshot	rs876661033
SNPdbe	rs876661033
MSV3d	rs876661033
GWAS Ctlg	rs876661033

Max Magnitude

0

ClinVar
Risk	rs876661033(-;-)
Alt	rs876661033(-;-)
Reference	Rs876661033(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MSH6
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.48026767delT
CLNSRC
CLNACC	RCV000214419.1,