rs267608118

Orientation

plus

Stabilized

plus

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

Make rs267608118(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47806454

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs267608118
dbSNP (classic)	rs267608118
ClinGen	rs267608118
ebi	rs267608118
HLI	rs267608118
Exac	rs267608118
Gnomad	rs267608118
Varsome	rs267608118
LitVar	rs267608118
Map	rs267608118
PheGenI	rs267608118
Biobank	rs267608118
1000 genomes	rs267608118
hgdp	rs267608118
ensembl	rs267608118
geneview	rs267608118
scholar	rs267608118
google	rs267608118
pharmgkb	rs267608118
gwascentral	rs267608118
openSNP	rs267608118
23andMe	rs267608118
SNPshot	rs267608118
SNPdbe	rs267608118
MSV3d	rs267608118
GWAS Ctlg	rs267608118

Max Magnitude

6

ClinVar
Risk	rs267608118(A;A)
Alt	rs267608118(A;A)
Reference	Rs267608118(-;-)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.48033593dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074937.2, RCV000214022.1, RCV000214836.2,