rs587779318

Orientation

plus

Stabilized

plus

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

Make rs587779318(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47798677

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587779318
dbSNP (classic)	rs587779318
ClinGen	rs587779318
ebi	rs587779318
HLI	rs587779318
Exac	rs587779318
Gnomad	rs587779318
Varsome	rs587779318
LitVar	rs587779318
Map	rs587779318
PheGenI	rs587779318
Biobank	rs587779318
1000 genomes	rs587779318
hgdp	rs587779318
ensembl	rs587779318
geneview	rs587779318
scholar	rs587779318
google	rs587779318
pharmgkb	rs587779318
gwascentral	rs587779318
openSNP	rs587779318
23andMe	rs587779318
SNPshot	rs587779318
SNPdbe	rs587779318
MSV3d	rs587779318
GWAS Ctlg	rs587779318

Max Magnitude

6

ClinVar
Risk	rs587779318(T;T)
Alt	rs587779318(T;T)
Reference	Rs587779318(C;C)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.48025816C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075025.2, RCV000412800.1,