rs878854491

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	Lynch syndrome mutation

Make rs878854491(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47377045

Gene	EPCAM, MIR559

is a	snp
is	mentioned by
dbSNP	rs878854491
dbSNP (classic)	rs878854491
ClinGen	rs878854491
ebi	rs878854491
HLI	rs878854491
Exac	rs878854491
Gnomad	rs878854491
Varsome	rs878854491
LitVar	rs878854491
Map	rs878854491
PheGenI	rs878854491
Biobank	rs878854491
1000 genomes	rs878854491
hgdp	rs878854491
ensembl	rs878854491
geneview	rs878854491
scholar	rs878854491
google	rs878854491
pharmgkb	rs878854491
gwascentral	rs878854491
openSNP	rs878854491
23andMe	rs878854491
SNPshot	rs878854491
SNPdbe	rs878854491
MSV3d	rs878854491
GWAS Ctlg	rs878854491

Max Magnitude

6

ClinVar
Risk	rs878854491(T;T)
Alt	rs878854491(T;T)
Reference	Rs878854491(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	EPCAM MIR559
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47604184C>T
CLNSRC
CLNACC	RCV000227834.1,