rs63751319

Orientation

plus

Stabilized

plus

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

Make rs63751319(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47806490

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs63751319
dbSNP (classic)	rs63751319
ClinGen	rs63751319
ebi	rs63751319
HLI	rs63751319
Exac	rs63751319
Gnomad	rs63751319
Varsome	rs63751319
LitVar	rs63751319
Map	rs63751319
PheGenI	rs63751319
Biobank	rs63751319
1000 genomes	rs63751319
hgdp	rs63751319
ensembl	rs63751319
geneview	rs63751319
scholar	rs63751319
google	rs63751319
pharmgkb	rs63751319
gwascentral	rs63751319
openSNP	rs63751319
23andMe	rs63751319
SNPshot	rs63751319
SNPdbe	rs63751319
MSV3d	rs63751319
GWAS Ctlg	rs63751319

Max Magnitude

6

ClinVar
Risk	rs63751319(-;-)
Alt	rs63751319(-;-)
Reference	Rs63751319(GGAGACT;GGAGACT)
Significance	Pathogenic
Disease	Lynch syndrome not provided Hereditary nonpolyposis colorectal cancer type 5 Hereditary cancer-predisposing syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Lynch syndrome not provided Hereditary nonpolyposis colorectal cancer type 5 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48033629_48033635delGGAGACT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074942.2, RCV000219135.2, RCV000409718.1, RCV000491396.1,