rs267607168

Orientation

plus

Stabilized

plus

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

Make rs267607168(C;C)

Make rs267607168(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160425122

Gene

VANGL2

is a	snp
is	mentioned by
dbSNP	rs267607168
dbSNP (classic)	rs267607168
ClinGen	rs267607168
ebi	rs267607168
HLI	rs267607168
Exac	rs267607168
Gnomad	rs267607168
Varsome	rs267607168
LitVar	rs267607168
Map	rs267607168
PheGenI	rs267607168
Biobank	rs267607168
1000 genomes	rs267607168
hgdp	rs267607168
ensembl	rs267607168
geneview	rs267607168
scholar	rs267607168
google	rs267607168
pharmgkb	rs267607168
gwascentral	rs267607168
openSNP	rs267607168
23andMe	rs267607168
SNPshot	rs267607168
SNPdbe	rs267607168
MSV3d	rs267607168
GWAS Ctlg	rs267607168

Max Magnitude

0

ClinVar
Risk	rs267607168(C;C)
Alt	rs267607168(C;C)
Reference	Rs267607168(T;T)
Significance	Other
Disease	Neural tube defects
Variation	info
Gene	VANGL2
CLNDBN	Neural tube defects, susceptibility to
Reversed	0
HGVS	NC_000001.10:g.160394912T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009620.5,