rs63751419

Orientation

plus

Stabilized

plus

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

Make rs63751419(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47800088

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63751419
dbSNP (classic)	rs63751419
ClinGen	rs63751419
ebi	rs63751419
HLI	rs63751419
Exac	rs63751419
Gnomad	rs63751419
Varsome	rs63751419
LitVar	rs63751419
Map	rs63751419
PheGenI	rs63751419
Biobank	rs63751419
1000 genomes	rs63751419
hgdp	rs63751419
ensembl	rs63751419
geneview	rs63751419
scholar	rs63751419
google	rs63751419
pharmgkb	rs63751419
gwascentral	rs63751419
openSNP	rs63751419
23andMe	rs63751419
SNPshot	rs63751419
SNPdbe	rs63751419
MSV3d	rs63751419
GWAS Ctlg	rs63751419

Max Magnitude

6

ClinVar
Risk	rs63751419(G;G) rs63751419(T;T)
Alt	rs63751419(G;G) rs63751419(T;T)
Reference	Rs63751419(C;C)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48027227C>G; NC_000002.11:g.48027227C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074717.2, RCV000129429.2,