rs751033488

Merged into

rs267608121

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs751033488(-;TCAG)

Make rs751033488(TCAG;TCAG)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47806630

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs751033488
dbSNP (classic)	rs751033488
ClinGen	rs751033488
ebi	rs751033488
HLI	rs751033488
Exac	rs751033488
Gnomad	rs751033488
Varsome	rs751033488
LitVar	rs751033488
Map	rs751033488
PheGenI	rs751033488
Biobank	rs751033488
1000 genomes	rs751033488
hgdp	rs751033488
ensembl	rs751033488
geneview	rs751033488
scholar	rs751033488
google	rs751033488
pharmgkb	rs751033488
gwascentral	rs751033488
openSNP	rs751033488
23andMe	rs751033488
SNPshot	rs751033488
SNPdbe	rs751033488
MSV3d	rs751033488
GWAS Ctlg	rs751033488

Status

Merged into rs267608121

Max Magnitude

0

ClinVar
Risk	rs751033488(TCAG;TCAG)
Alt	rs751033488(TCAG;TCAG)
Reference	Rs751033488(;)
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.48033773_48033776dupGTCA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074964.3, RCV000131963.5, RCV000202165.1,