rs1057524821

Orientation

minus

Stabilized

minus

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

Make rs1057524821(C;C)

Make rs1057524821(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

55228900

Gene

TCF4

is a	snp
is	mentioned by
dbSNP	rs1057524821
dbSNP (classic)	rs1057524821
ClinGen	rs1057524821
ebi	rs1057524821
HLI	rs1057524821
Exac	rs1057524821
Gnomad	rs1057524821
Varsome	rs1057524821
LitVar	rs1057524821
Map	rs1057524821
PheGenI	rs1057524821
Biobank	rs1057524821
1000 genomes	rs1057524821
hgdp	rs1057524821
ensembl	rs1057524821
geneview	rs1057524821
scholar	rs1057524821
google	rs1057524821
pharmgkb	rs1057524821
gwascentral	rs1057524821
openSNP	rs1057524821
23andMe	rs1057524821
SNPshot	rs1057524821
SNPdbe	rs1057524821
MSV3d	rs1057524821
GWAS Ctlg	rs1057524821

Max Magnitude

0

ClinVar
Risk	rs1057524821(C;C)
Alt	rs1057524821(C;C)
Reference	Rs1057524821(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TCF4
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.52896131A>G
CLNSRC
CLNACC	RCV000418798.1,