rs796053424

Orientation

minus

Stabilized

minus

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

Make rs796053424(-;AG)

Make rs796053424(AG;AG)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

55350390

Gene

TCF4

is a	snp
is	mentioned by
dbSNP	rs796053424
dbSNP (classic)	rs796053424
ClinGen	rs796053424
ebi	rs796053424
HLI	rs796053424
Exac	rs796053424
Gnomad	rs796053424
Varsome	rs796053424
LitVar	rs796053424
Map	rs796053424
PheGenI	rs796053424
Biobank	rs796053424
1000 genomes	rs796053424
hgdp	rs796053424
ensembl	rs796053424
geneview	rs796053424
scholar	rs796053424
google	rs796053424
pharmgkb	rs796053424
gwascentral	rs796053424
openSNP	rs796053424
23andMe	rs796053424
SNPshot	rs796053424
SNPdbe	rs796053424
MSV3d	rs796053424
GWAS Ctlg	rs796053424

Max Magnitude

0

ClinVar
Risk	rs796053424(AG;AG)
Alt	rs796053424(AG;AG)
Reference	Rs796053424(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TCF4
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.53017622_53017623dupCT
CLNSRC
CLNACC	RCV000189729.1,