rs121918219

Orientation

plus

Stabilized

plus

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

Make rs121918219(A;A)

Make rs121918219(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

115682372

Gene

VANGL1

is a	snp
is	mentioned by
dbSNP	rs121918219
dbSNP (classic)	rs121918219
ClinGen	rs121918219
ebi	rs121918219
HLI	rs121918219
Exac	rs121918219
Gnomad	rs121918219
Varsome	rs121918219
LitVar	rs121918219
Map	rs121918219
PheGenI	rs121918219
Biobank	rs121918219
1000 genomes	rs121918219
hgdp	rs121918219
ensembl	rs121918219
geneview	rs121918219
scholar	rs121918219
google	rs121918219
pharmgkb	rs121918219
gwascentral	rs121918219
openSNP	rs121918219
23andMe	rs121918219
SNPshot	rs121918219
SNPdbe	rs121918219
MSV3d	rs121918219
GWAS Ctlg	rs121918219

Max Magnitude

0

OMIM	610132
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121918219(A;A)
Alt	rs121918219(A;A)
Reference	Rs121918219(G;G)
Significance	Other
Disease	Neural tube defects
Variation	info
Gene	VANGL1
CLNDBN	Neural tube defects, susceptibility to
Reversed	0
HGVS	NC_000001.10:g.116224993G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001412.4,