rs796053420

Orientation

minus

Stabilized

minus

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

Make rs796053420(C;G)

Make rs796053420(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

55232524

Gene

TCF4

is a	snp
is	mentioned by
dbSNP	rs796053420
dbSNP (classic)	rs796053420
ClinGen	rs796053420
ebi	rs796053420
HLI	rs796053420
Exac	rs796053420
Gnomad	rs796053420
Varsome	rs796053420
LitVar	rs796053420
Map	rs796053420
PheGenI	rs796053420
Biobank	rs796053420
1000 genomes	rs796053420
hgdp	rs796053420
ensembl	rs796053420
geneview	rs796053420
scholar	rs796053420
google	rs796053420
pharmgkb	rs796053420
gwascentral	rs796053420
openSNP	rs796053420
23andMe	rs796053420
SNPshot	rs796053420
SNPdbe	rs796053420
MSV3d	rs796053420
GWAS Ctlg	rs796053420

Max Magnitude

0

ClinVar
Risk	rs796053420(G;G)
Alt	rs796053420(G;G)
Reference	Rs796053420(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TCF4
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.52899755G>C
CLNSRC
CLNACC	RCV000189724.1,