rs267607167

Orientation

plus

Stabilized

plus

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

Make rs267607167(C;T)

Make rs267607167(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160421171

Gene

VANGL2

is a	snp
is	mentioned by
dbSNP	rs267607167
dbSNP (classic)	rs267607167
ClinGen	rs267607167
ebi	rs267607167
HLI	rs267607167
Exac	rs267607167
Gnomad	rs267607167
Varsome	rs267607167
LitVar	rs267607167
Map	rs267607167
PheGenI	rs267607167
Biobank	rs267607167
1000 genomes	rs267607167
hgdp	rs267607167
ensembl	rs267607167
geneview	rs267607167
scholar	rs267607167
google	rs267607167
pharmgkb	rs267607167
gwascentral	rs267607167
openSNP	rs267607167
23andMe	rs267607167
SNPshot	rs267607167
SNPdbe	rs267607167
MSV3d	rs267607167
GWAS Ctlg	rs267607167

Max Magnitude

0

ClinVar
Risk	rs267607167(G;G) rs267607167(T;T)
Alt	rs267607167(G;G) rs267607167(T;T)
Reference	Rs267607167(C;C)
Significance	Other
Disease	Neural tube defects
Variation	info
Gene	VANGL2
CLNDBN	Neural tube defects, susceptibility to
Reversed	0
HGVS	NC_000001.10:g.160390961C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009619.7,