rs587782326

Orientation

plus

Stabilized

plus

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

Make rs587782326(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47806629

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs587782326
dbSNP (classic)	rs587782326
ClinGen	rs587782326
ebi	rs587782326
HLI	rs587782326
Exac	rs587782326
Gnomad	rs587782326
Varsome	rs587782326
LitVar	rs587782326
Map	rs587782326
PheGenI	rs587782326
Biobank	rs587782326
1000 genomes	rs587782326
hgdp	rs587782326
ensembl	rs587782326
geneview	rs587782326
scholar	rs587782326
google	rs587782326
pharmgkb	rs587782326
gwascentral	rs587782326
openSNP	rs587782326
23andMe	rs587782326
SNPshot	rs587782326
SNPdbe	rs587782326
MSV3d	rs587782326
GWAS Ctlg	rs587782326

Max Magnitude

6

ClinVar
Risk	rs587782326(A;A)
Alt	rs587782326(A;A)
Reference	Rs587782326(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48033768dupA
CLNSRC
CLNACC	RCV000131234.2,