rs730881829

Orientation

plus

Stabilized

plus

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

Make rs730881829(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47806247

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs730881829
dbSNP (classic)	rs730881829
ClinGen	rs730881829
ebi	rs730881829
HLI	rs730881829
Exac	rs730881829
Gnomad	rs730881829
Varsome	rs730881829
LitVar	rs730881829
Map	rs730881829
PheGenI	rs730881829
Biobank	rs730881829
1000 genomes	rs730881829
hgdp	rs730881829
ensembl	rs730881829
geneview	rs730881829
scholar	rs730881829
google	rs730881829
pharmgkb	rs730881829
gwascentral	rs730881829
openSNP	rs730881829
23andMe	rs730881829
SNPshot	rs730881829
SNPdbe	rs730881829
MSV3d	rs730881829
GWAS Ctlg	rs730881829

Max Magnitude

6

ClinVar
Risk	rs730881829(-;-)
Alt	rs730881829(-;-)
Reference	Rs730881829(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48033386delA
CLNSRC
CLNACC	RCV000160745.1, RCV000205295.1,