rs63751077

Orientation

plus

Stabilized

plus

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

Make rs63751077(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47796035

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63751077
dbSNP (classic)	rs63751077
ClinGen	rs63751077
ebi	rs63751077
HLI	rs63751077
Exac	rs63751077
Gnomad	rs63751077
Varsome	rs63751077
LitVar	rs63751077
Map	rs63751077
PheGenI	rs63751077
Biobank	rs63751077
1000 genomes	rs63751077
hgdp	rs63751077
ensembl	rs63751077
geneview	rs63751077
scholar	rs63751077
google	rs63751077
pharmgkb	rs63751077
gwascentral	rs63751077
openSNP	rs63751077
23andMe	rs63751077
SNPshot	rs63751077
SNPdbe	rs63751077
MSV3d	rs63751077
GWAS Ctlg	rs63751077

Max Magnitude

6

c.599C>A (p.Ser200Ter)

23andMe name: i5901102

ClinVar
Risk	rs63751077(A;A) rs63751077(G;G)
Alt	rs63751077(A;A) rs63751077(G;G)
Reference	Rs63751077(C;C)
Significance	Pathogenic
Disease	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48023174C>A; NC_000002.11:g.48023174C>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075008.2, RCV000217643.1, RCV000491993.1,