rs866771359

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;T)	6	Lynch syndrome
(T;T)	0	common in clinvar

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47806496

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs866771359
dbSNP (classic)	rs866771359
ClinGen	rs866771359
ebi	rs866771359
HLI	rs866771359
Exac	rs866771359
Gnomad	rs866771359
Varsome	rs866771359
LitVar	rs866771359
Map	rs866771359
PheGenI	rs866771359
Biobank	rs866771359
1000 genomes	rs866771359
hgdp	rs866771359
ensembl	rs866771359
geneview	rs866771359
scholar	rs866771359
google	rs866771359
pharmgkb	rs866771359
gwascentral	rs866771359
openSNP	rs866771359
23andMe	rs866771359
SNPshot	rs866771359
SNPdbe	rs866771359
MSV3d	rs866771359
GWAS Ctlg	rs866771359

Max Magnitude

6

ClinVar
Risk	rs866771359(ATTA;ATTA) Rs866771359(T;T)
Alt	rs866771359(ATTA;ATTA) Rs866771359(T;T)
Reference	Rs866771359(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48033635dupT
CLNSRC
CLNACC	RCV000216834.1,