rs1057521070

Orientation

minus

Stabilized

minus

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

Make rs1057521070(A;A)

Make rs1057521070(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

55228999

Gene

TCF4

is a	snp
is	mentioned by
dbSNP	rs1057521070
dbSNP (classic)	rs1057521070
ClinGen	rs1057521070
ebi	rs1057521070
HLI	rs1057521070
Exac	rs1057521070
Gnomad	rs1057521070
Varsome	rs1057521070
LitVar	rs1057521070
Map	rs1057521070
PheGenI	rs1057521070
Biobank	rs1057521070
1000 genomes	rs1057521070
hgdp	rs1057521070
ensembl	rs1057521070
geneview	rs1057521070
scholar	rs1057521070
google	rs1057521070
pharmgkb	rs1057521070
gwascentral	rs1057521070
openSNP	rs1057521070
23andMe	rs1057521070
SNPshot	rs1057521070
SNPdbe	rs1057521070
MSV3d	rs1057521070
GWAS Ctlg	rs1057521070

Max Magnitude

0

ClinVar
Risk	rs1057521070(A;A)
Alt	rs1057521070(A;A)
Reference	Rs1057521070(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TCF4
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.52896230C>T
CLNSRC
CLNACC	RCV000431775.1,