rs587779237

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TG)	6	Lynch syndrome, pathogenic mutation
(TG;TG)	0	common in clinvar

Make rs587779237(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47800362

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587779237
dbSNP (classic)	rs587779237
ClinGen	rs587779237
ebi	rs587779237
HLI	rs587779237
Exac	rs587779237
Gnomad	rs587779237
Varsome	rs587779237
LitVar	rs587779237
Map	rs587779237
PheGenI	rs587779237
Biobank	rs587779237
1000 genomes	rs587779237
hgdp	rs587779237
ensembl	rs587779237
geneview	rs587779237
scholar	rs587779237
google	rs587779237
pharmgkb	rs587779237
gwascentral	rs587779237
openSNP	rs587779237
23andMe	rs587779237
SNPshot	rs587779237
SNPdbe	rs587779237
MSV3d	rs587779237
GWAS Ctlg	rs587779237

Max Magnitude

6

ClinVar
Risk	rs587779237(-;-)
Alt	rs587779237(-;-)
Reference	Rs587779237(TG;TG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48027501_48027502delTG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074742.2,