rs876660150

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs876660150(-;TT)

Make rs876660150(TT;TT)

Reference

GRCh38.p2 38.2/147

Chromosome

18

Position

51078394

Gene

SMAD4

is a	snp
is	mentioned by
dbSNP	rs876660150
dbSNP (classic)	rs876660150
ClinGen	rs876660150
ebi	rs876660150
HLI	rs876660150
Exac	rs876660150
Gnomad	rs876660150
Varsome	rs876660150
LitVar	rs876660150
Map	rs876660150
PheGenI	rs876660150
Biobank	rs876660150
1000 genomes	rs876660150
hgdp	rs876660150
ensembl	rs876660150
geneview	rs876660150
scholar	rs876660150
google	rs876660150
pharmgkb	rs876660150
gwascentral	rs876660150
openSNP	rs876660150
23andMe	rs876660150
SNPshot	rs876660150
SNPdbe	rs876660150
MSV3d	rs876660150
GWAS Ctlg	rs876660150

Max Magnitude

0

ClinVar
Risk	rs876660150(TT;TT)
Alt	rs876660150(TT;TT)
Reference	Rs876660150(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SMAD4
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000018.9:g.48604763_48604764dupTT
CLNSRC
CLNACC	RCV000220401.1,