rs878853149

Orientation

minus

Stabilized

minus

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

Make rs878853149(C;T)

Make rs878853149(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

18

Position

55350388

Gene

TCF4

is a	snp
is	mentioned by
dbSNP	rs878853149
dbSNP (classic)	rs878853149
ClinGen	rs878853149
ebi	rs878853149
HLI	rs878853149
Exac	rs878853149
Gnomad	rs878853149
Varsome	rs878853149
LitVar	rs878853149
Map	rs878853149
PheGenI	rs878853149
Biobank	rs878853149
1000 genomes	rs878853149
hgdp	rs878853149
ensembl	rs878853149
geneview	rs878853149
scholar	rs878853149
google	rs878853149
pharmgkb	rs878853149
gwascentral	rs878853149
openSNP	rs878853149
23andMe	rs878853149
SNPshot	rs878853149
SNPdbe	rs878853149
MSV3d	rs878853149
GWAS Ctlg	rs878853149

Max Magnitude

0

ClinVar
Risk	rs878853149(T;T)
Alt	rs878853149(T;T)
Reference	Rs878853149(C;C)
Significance	Pathogenic
Disease	Intellectual disability
Variation	info
Gene	TCF4
CLNDBN	Intellectual disability
Reversed	1
HGVS	NC_000018.9:g.53017619G>A
CLNSRC
CLNACC	RCV000224478.1,