rs796053418

Orientation

minus

Stabilized

minus

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

Make rs796053418(C;T)

Make rs796053418(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

55232588

Gene

TCF4

is a	snp
is	mentioned by
dbSNP	rs796053418
dbSNP (classic)	rs796053418
ClinGen	rs796053418
ebi	rs796053418
HLI	rs796053418
Exac	rs796053418
Gnomad	rs796053418
Varsome	rs796053418
LitVar	rs796053418
Map	rs796053418
PheGenI	rs796053418
Biobank	rs796053418
1000 genomes	rs796053418
hgdp	rs796053418
ensembl	rs796053418
geneview	rs796053418
scholar	rs796053418
google	rs796053418
pharmgkb	rs796053418
gwascentral	rs796053418
openSNP	rs796053418
23andMe	rs796053418
SNPshot	rs796053418
SNPdbe	rs796053418
MSV3d	rs796053418
GWAS Ctlg	rs796053418

Max Magnitude

0

ClinVar
Risk	rs796053418(T;T)
Alt	rs796053418(T;T)
Reference	Rs796053418(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TCF4
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.52899819G>A
CLNSRC
CLNACC	RCV000189722.1,