rs121909121

Orientation

minus

Stabilized

minus

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

Make rs121909121(A;A)

Make rs121909121(A;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

55228987

Gene

TCF4

is a	snp
is	mentioned by
dbSNP	rs121909121
dbSNP (classic)	rs121909121
ClinGen	rs121909121
ebi	rs121909121
HLI	rs121909121
Exac	rs121909121
Gnomad	rs121909121
Varsome	rs121909121
LitVar	rs121909121
Map	rs121909121
PheGenI	rs121909121
Biobank	rs121909121
1000 genomes	rs121909121
hgdp	rs121909121
ensembl	rs121909121
geneview	rs121909121
scholar	rs121909121
google	rs121909121
pharmgkb	rs121909121
gwascentral	rs121909121
openSNP	rs121909121
23andMe	rs121909121
SNPshot	rs121909121
SNPdbe	rs121909121
MSV3d	rs121909121
GWAS Ctlg	rs121909121

Max Magnitude

0

OMIM	602272
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909121(A;A)
Alt	rs121909121(A;A)
Reference	Rs121909121(G;G)
Significance	Pathogenic
Disease	Pitt-Hopkins syndrome not provided
Variation	info
Gene	TCF4
CLNDBN	Pitt-Hopkins syndrome not provided
Reversed	1
HGVS	NC_000018.9:g.52896218C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007796.3, RCV000189725.2,