rs1057518339

Orientation

minus

Stabilized

minus

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

Make rs1057518339(C;G)

Make rs1057518339(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

55259981

Gene

TCF4

is a	snp
is	mentioned by
dbSNP	rs1057518339
dbSNP (classic)	rs1057518339
ClinGen	rs1057518339
ebi	rs1057518339
HLI	rs1057518339
Exac	rs1057518339
Gnomad	rs1057518339
Varsome	rs1057518339
LitVar	rs1057518339
Map	rs1057518339
PheGenI	rs1057518339
Biobank	rs1057518339
1000 genomes	rs1057518339
hgdp	rs1057518339
ensembl	rs1057518339
geneview	rs1057518339
scholar	rs1057518339
google	rs1057518339
pharmgkb	rs1057518339
gwascentral	rs1057518339
openSNP	rs1057518339
23andMe	rs1057518339
SNPshot	rs1057518339
SNPdbe	rs1057518339
MSV3d	rs1057518339
GWAS Ctlg	rs1057518339

Max Magnitude

0

ClinVar
Risk	rs1057518339(G;G)
Alt	rs1057518339(G;G)
Reference	Rs1057518339(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TCF4
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.52927212G>C
CLNSRC
CLNACC	RCV000413573.1,