rs587779252

Orientation

plus

Stabilized

plus

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

Make rs587779252(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47801003

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587779252
dbSNP (classic)	rs587779252
ClinGen	rs587779252
ebi	rs587779252
HLI	rs587779252
Exac	rs587779252
Gnomad	rs587779252
Varsome	rs587779252
LitVar	rs587779252
Map	rs587779252
PheGenI	rs587779252
Biobank	rs587779252
1000 genomes	rs587779252
hgdp	rs587779252
ensembl	rs587779252
geneview	rs587779252
scholar	rs587779252
google	rs587779252
pharmgkb	rs587779252
gwascentral	rs587779252
openSNP	rs587779252
23andMe	rs587779252
SNPshot	rs587779252
SNPdbe	rs587779252
MSV3d	rs587779252
GWAS Ctlg	rs587779252

Max Magnitude

6

ClinVar
Risk	rs587779252(A;A)
Alt	rs587779252(A;A)
Reference	Rs587779252(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48028142G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074796.2,