rs763673818

Merged into

rs63750767

Orientation

plus

Stabilized

plus

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

Make rs763673818(-;TCAAAAGGGACATAGAAAA)

Make rs763673818(TCAAAAGGGACATAGAAAA;TCAAAAGGGACATAGAAAA)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47806588

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs763673818
dbSNP (classic)	rs763673818
ClinGen	rs763673818
ebi	rs763673818
HLI	rs763673818
Exac	rs763673818
Gnomad	rs763673818
Varsome	rs763673818
LitVar	rs763673818
Map	rs763673818
PheGenI	rs763673818
Biobank	rs763673818
1000 genomes	rs763673818
hgdp	rs763673818
ensembl	rs763673818
geneview	rs763673818
scholar	rs763673818
google	rs763673818
pharmgkb	rs763673818
gwascentral	rs763673818
openSNP	rs763673818
23andMe	rs763673818
SNPshot	rs763673818
SNPdbe	rs763673818
MSV3d	rs763673818
GWAS Ctlg	rs763673818

Status

Merged into rs63750767

Max Magnitude

0

ClinVar
Risk	rs763673818(TCAAAAGGGACATAGAAAA;TCAAAAGGGACATAGAAAA)
Alt	rs763673818(TCAAAAGGGACATAGAAAA;TCAAAAGGGACATAGAAAA)
Reference	Rs763673818(;)
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.48033728_48033746dup19
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074954.2, RCV000129554.5, RCV000202115.1,