rs63750139

Orientation

plus

Stabilized

plus

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

Make rs63750139(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47806488

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs63750139
dbSNP (classic)	rs63750139
ClinGen	rs63750139
ebi	rs63750139
HLI	rs63750139
Exac	rs63750139
Gnomad	rs63750139
Varsome	rs63750139
LitVar	rs63750139
Map	rs63750139
PheGenI	rs63750139
Biobank	rs63750139
1000 genomes	rs63750139
hgdp	rs63750139
ensembl	rs63750139
geneview	rs63750139
scholar	rs63750139
google	rs63750139
pharmgkb	rs63750139
gwascentral	rs63750139
openSNP	rs63750139
23andMe	rs63750139
SNPshot	rs63750139
SNPdbe	rs63750139
MSV3d	rs63750139
GWAS Ctlg	rs63750139

Max Magnitude

6

ClinVar
Risk	rs63750139(T;T)
Alt	rs63750139(T;T)
Reference	Rs63750139(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48033627C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074940.2,