rs121918220

Orientation

plus

Stabilized

plus

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

Make rs121918220(C;C)

Make rs121918220(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

115683980

Gene

VANGL1

is a	snp
is	mentioned by
dbSNP	rs121918220
dbSNP (classic)	rs121918220
ClinGen	rs121918220
ebi	rs121918220
HLI	rs121918220
Exac	rs121918220
Gnomad	rs121918220
Varsome	rs121918220
LitVar	rs121918220
Map	rs121918220
PheGenI	rs121918220
Biobank	rs121918220
1000 genomes	rs121918220
hgdp	rs121918220
ensembl	rs121918220
geneview	rs121918220
scholar	rs121918220
google	rs121918220
pharmgkb	rs121918220
gwascentral	rs121918220
openSNP	rs121918220
23andMe	rs121918220
SNPshot	rs121918220
SNPdbe	rs121918220
MSV3d	rs121918220
GWAS Ctlg	rs121918220

Max Magnitude

0

OMIM	610132
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121918220(C;C)
Alt	rs121918220(C;C)
Reference	Rs121918220(T;T)
Significance	Other
Disease	Neural tube defects
Variation	info
Gene	VANGL1
CLNDBN	Neural tube defects, susceptibility to
Reversed	0
HGVS	NC_000001.10:g.116226601T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001413.4,