rs63749999

Orientation

plus

Stabilized

plus

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

Make rs63749999(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47801086

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63749999
dbSNP (classic)	rs63749999
ClinGen	rs63749999
ebi	rs63749999
HLI	rs63749999
Exac	rs63749999
Gnomad	rs63749999
Varsome	rs63749999
LitVar	rs63749999
Map	rs63749999
PheGenI	rs63749999
Biobank	rs63749999
1000 genomes	rs63749999
hgdp	rs63749999
ensembl	rs63749999
geneview	rs63749999
scholar	rs63749999
google	rs63749999
pharmgkb	rs63749999
gwascentral	rs63749999
openSNP	rs63749999
23andMe	rs63749999
SNPshot	rs63749999
SNPdbe	rs63749999
MSV3d	rs63749999
GWAS Ctlg	rs63749999

Max Magnitude

6

ClinVar
Risk	rs63749999(T;T)
Alt	rs63749999(T;T)
Reference	Rs63749999(C;C)
Significance	Pathogenic
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.48028225C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074803.2, RCV000223452.2, RCV000484829.1,