rs63750909

Orientation

plus

Stabilized

plus

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

Make rs63750909(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47799427

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63750909
dbSNP (classic)	rs63750909
ClinGen	rs63750909
ebi	rs63750909
HLI	rs63750909
Exac	rs63750909
Gnomad	rs63750909
Varsome	rs63750909
LitVar	rs63750909
Map	rs63750909
PheGenI	rs63750909
Biobank	rs63750909
1000 genomes	rs63750909
hgdp	rs63750909
ensembl	rs63750909
geneview	rs63750909
scholar	rs63750909
google	rs63750909
pharmgkb	rs63750909
gwascentral	rs63750909
openSNP	rs63750909
23andMe	rs63750909
SNPshot	rs63750909
SNPdbe	rs63750909
MSV3d	rs63750909
GWAS Ctlg	rs63750909

Max Magnitude

6

ClinVar
Risk	rs63750909(A;A) rs63750909(G;G) rs63750909(T;T)
Alt	rs63750909(A;A) rs63750909(G;G) rs63750909(T;T)
Reference	Rs63750909(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not specified Lynch syndrome not provided Hereditary nonpolyposis colorectal cancer type 5
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome not specified Lynch syndrome not provided Hereditary nonpolyposis colorectal cancer type 5
Reversed	0
HGVS	NC_000002.11:g.48026566C>A; NC_000002.11:g.48026566C>G; NC_000002.11:g.48026566C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000163642.1, RCV000417944.1, RCV000480474.1, RCV000074656.2, RCV000215386.2, RCV000410127.1, RCV000491001.1,