rs796053427

Orientation

minus

Stabilized

minus

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

Make rs796053427(-;-)

Make rs796053427(-;AGGGGCAGAGTGTC)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

55232640

Gene

TCF4

is a	snp
is	mentioned by
dbSNP	rs796053427
dbSNP (classic)	rs796053427
ClinGen	rs796053427
ebi	rs796053427
HLI	rs796053427
Exac	rs796053427
Gnomad	rs796053427
Varsome	rs796053427
LitVar	rs796053427
Map	rs796053427
PheGenI	rs796053427
Biobank	rs796053427
1000 genomes	rs796053427
hgdp	rs796053427
ensembl	rs796053427
geneview	rs796053427
scholar	rs796053427
google	rs796053427
pharmgkb	rs796053427
gwascentral	rs796053427
openSNP	rs796053427
23andMe	rs796053427
SNPshot	rs796053427
SNPdbe	rs796053427
MSV3d	rs796053427
GWAS Ctlg	rs796053427

Max Magnitude

0

ClinVar
Risk	rs796053427(-;-)
Alt	rs796053427(-;-)
Reference	Rs796053427(AGGGGCAGAGTGTC;AGGGGCAGAGTGTC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TCF4
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.52899871_52899884delGACACTCTGCCCCT
CLNSRC
CLNACC	RCV000189732.1,