rs730881828

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;AC)	6	Lynch syndrome

Make rs730881828(AC;AC)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47804995

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs730881828
dbSNP (classic)	rs730881828
ClinGen	rs730881828
ebi	rs730881828
HLI	rs730881828
Exac	rs730881828
Gnomad	rs730881828
Varsome	rs730881828
LitVar	rs730881828
Map	rs730881828
PheGenI	rs730881828
Biobank	rs730881828
1000 genomes	rs730881828
hgdp	rs730881828
ensembl	rs730881828
geneview	rs730881828
scholar	rs730881828
google	rs730881828
pharmgkb	rs730881828
gwascentral	rs730881828
openSNP	rs730881828
23andMe	rs730881828
SNPshot	rs730881828
SNPdbe	rs730881828
MSV3d	rs730881828
GWAS Ctlg	rs730881828

Max Magnitude

6

ClinVar
Risk	rs730881828(AC;AC)
Alt	rs730881828(AC;AC)
Reference	Rs730881828(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48032133_48032134dupAC
CLNSRC
CLNACC	RCV000160744.1,