rs878854488

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	3	Carrier of an infancy diarrhea mutation
(G;G)	0	common in clinvar

Make rs878854488(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47375237

Gene

EPCAM

is a	snp
is	mentioned by
dbSNP	rs878854488
dbSNP (classic)	rs878854488
ClinGen	rs878854488
ebi	rs878854488
HLI	rs878854488
Exac	rs878854488
Gnomad	rs878854488
Varsome	rs878854488
LitVar	rs878854488
Map	rs878854488
PheGenI	rs878854488
Biobank	rs878854488
1000 genomes	rs878854488
hgdp	rs878854488
ensembl	rs878854488
geneview	rs878854488
scholar	rs878854488
google	rs878854488
pharmgkb	rs878854488
gwascentral	rs878854488
openSNP	rs878854488
23andMe	rs878854488
SNPshot	rs878854488
SNPdbe	rs878854488
MSV3d	rs878854488
GWAS Ctlg	rs878854488

Max Magnitude

3

ClinVar
Risk	rs878854488(A;A)
Alt	rs878854488(A;A)
Reference	Rs878854488(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	EPCAM
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47602376G>A
CLNSRC
CLNACC	RCV000229611.1,