rs876661125

Orientation

plus

Stabilized

plus

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

Make rs876661125(-;-)

Make rs876661125(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47791124

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs876661125
dbSNP (classic)	rs876661125
ClinGen	rs876661125
ebi	rs876661125
HLI	rs876661125
Exac	rs876661125
Gnomad	rs876661125
Varsome	rs876661125
LitVar	rs876661125
Map	rs876661125
PheGenI	rs876661125
Biobank	rs876661125
1000 genomes	rs876661125
hgdp	rs876661125
ensembl	rs876661125
geneview	rs876661125
scholar	rs876661125
google	rs876661125
pharmgkb	rs876661125
gwascentral	rs876661125
openSNP	rs876661125
23andMe	rs876661125
SNPshot	rs876661125
SNPdbe	rs876661125
MSV3d	rs876661125
GWAS Ctlg	rs876661125

Max Magnitude

0

ClinVar
Risk	rs876661125(-;-)
Alt	rs876661125(-;-)
Reference	Rs876661125(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MSH6
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.48018263delG
CLNSRC
CLNACC	RCV000216047.1,