rs878853729

Orientation

plus

Stabilized

plus

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

Make rs878853729(-;G)

Make rs878853729(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47801146

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs878853729
dbSNP (classic)	rs878853729
ClinGen	rs878853729
ebi	rs878853729
HLI	rs878853729
Exac	rs878853729
Gnomad	rs878853729
Varsome	rs878853729
LitVar	rs878853729
Map	rs878853729
PheGenI	rs878853729
Biobank	rs878853729
1000 genomes	rs878853729
hgdp	rs878853729
ensembl	rs878853729
geneview	rs878853729
scholar	rs878853729
google	rs878853729
pharmgkb	rs878853729
gwascentral	rs878853729
openSNP	rs878853729
23andMe	rs878853729
SNPshot	rs878853729
SNPdbe	rs878853729
MSV3d	rs878853729
GWAS Ctlg	rs878853729

Max Magnitude

0

ClinVar
Risk	rs878853729(G;G)
Alt	rs878853729(G;G)
Reference	Rs878853729(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48028285dupG
CLNSRC
CLNACC	RCV000233953.1,