rs796053428

Orientation

minus

Stabilized

minus

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

Make rs796053428(-;GGCC)

Make rs796053428(GGCC;GGCC)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

55228271

Gene

TCF4

is a	snp
is	mentioned by
dbSNP	rs796053428
dbSNP (classic)	rs796053428
ClinGen	rs796053428
ebi	rs796053428
HLI	rs796053428
Exac	rs796053428
Gnomad	rs796053428
Varsome	rs796053428
LitVar	rs796053428
Map	rs796053428
PheGenI	rs796053428
Biobank	rs796053428
1000 genomes	rs796053428
hgdp	rs796053428
ensembl	rs796053428
geneview	rs796053428
scholar	rs796053428
google	rs796053428
pharmgkb	rs796053428
gwascentral	rs796053428
openSNP	rs796053428
23andMe	rs796053428
SNPshot	rs796053428
SNPdbe	rs796053428
MSV3d	rs796053428
GWAS Ctlg	rs796053428

Max Magnitude

0

ClinVar
Risk	rs796053428(GGCC;GGCC)
Alt	rs796053428(GGCC;GGCC)
Reference	Rs796053428(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TCF4
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.52895503_52895506dupGGCC
CLNSRC
CLNACC	RCV000189733.1,