rs267608124

Orientation

plus

Stabilized

plus

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

Make rs267608124(ATCA;ATCA)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47806634

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs267608124
dbSNP (classic)	rs267608124
ClinGen	rs267608124
ebi	rs267608124
HLI	rs267608124
Exac	rs267608124
Gnomad	rs267608124
Varsome	rs267608124
LitVar	rs267608124
Map	rs267608124
PheGenI	rs267608124
Biobank	rs267608124
1000 genomes	rs267608124
hgdp	rs267608124
ensembl	rs267608124
geneview	rs267608124
scholar	rs267608124
google	rs267608124
pharmgkb	rs267608124
gwascentral	rs267608124
openSNP	rs267608124
23andMe	rs267608124
SNPshot	rs267608124
SNPdbe	rs267608124
MSV3d	rs267608124
GWAS Ctlg	rs267608124

Max Magnitude

6

ClinVar
Risk	rs267608124(ATCA;ATCA)
Alt	rs267608124(ATCA;ATCA)
Reference	Rs267608124(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48033773_48033774insATCA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074963.2,