rs587779296

Orientation

plus

Stabilized

plus

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

Make rs587779296(ATCTCCCA;ATCTCCCA)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47806577

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs587779296
dbSNP (classic)	rs587779296
ClinGen	rs587779296
ebi	rs587779296
HLI	rs587779296
Exac	rs587779296
Gnomad	rs587779296
Varsome	rs587779296
LitVar	rs587779296
Map	rs587779296
PheGenI	rs587779296
Biobank	rs587779296
1000 genomes	rs587779296
hgdp	rs587779296
ensembl	rs587779296
geneview	rs587779296
scholar	rs587779296
google	rs587779296
pharmgkb	rs587779296
gwascentral	rs587779296
openSNP	rs587779296
23andMe	rs587779296
SNPshot	rs587779296
SNPdbe	rs587779296
MSV3d	rs587779296
GWAS Ctlg	rs587779296

Max Magnitude

6

ClinVar
Risk	rs587779296(AATCTCCC;AATCTCCC)
Alt	rs587779296(AATCTCCC;AATCTCCC)
Reference	Rs587779296(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48033709_48033716dupATCTCCCA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074949.2,