rs587779212

Orientation

plus

Stabilized

plus

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

Make rs587779212(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47799466

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587779212
dbSNP (classic)	rs587779212
ClinGen	rs587779212
ebi	rs587779212
HLI	rs587779212
Exac	rs587779212
Gnomad	rs587779212
Varsome	rs587779212
LitVar	rs587779212
Map	rs587779212
PheGenI	rs587779212
Biobank	rs587779212
1000 genomes	rs587779212
hgdp	rs587779212
ensembl	rs587779212
geneview	rs587779212
scholar	rs587779212
google	rs587779212
pharmgkb	rs587779212
gwascentral	rs587779212
openSNP	rs587779212
23andMe	rs587779212
SNPshot	rs587779212
SNPdbe	rs587779212
MSV3d	rs587779212
GWAS Ctlg	rs587779212

Max Magnitude

6

ClinVar
Risk	rs587779212(T;T)
Alt	rs587779212(T;T)
Reference	Rs587779212(C;C)
Significance	Other
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.48026605C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074659.2, RCV000131420.4, RCV000202276.3,