rs587779234

Orientation

plus

Stabilized

plus

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

Make rs587779234(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47800313

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587779234
dbSNP (classic)	rs587779234
ClinGen	rs587779234
ebi	rs587779234
HLI	rs587779234
Exac	rs587779234
Gnomad	rs587779234
Varsome	rs587779234
LitVar	rs587779234
Map	rs587779234
PheGenI	rs587779234
Biobank	rs587779234
1000 genomes	rs587779234
hgdp	rs587779234
ensembl	rs587779234
geneview	rs587779234
scholar	rs587779234
google	rs587779234
pharmgkb	rs587779234
gwascentral	rs587779234
openSNP	rs587779234
23andMe	rs587779234
SNPshot	rs587779234
SNPdbe	rs587779234
MSV3d	rs587779234
GWAS Ctlg	rs587779234

Max Magnitude

6

ClinVar
Risk	rs587779234(A;A)
Alt	rs587779234(A;A)
Reference	Rs587779234(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48027452G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074736.2,