rs387907204

Orientation

minus

Stabilized

minus

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

Make rs387907204(C;T)

Make rs387907204(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

49812733

Gene

FUZ

is a	snp
is	mentioned by
dbSNP	rs387907204
dbSNP (classic)	rs387907204
ClinGen	rs387907204
ebi	rs387907204
HLI	rs387907204
Exac	rs387907204
Gnomad	rs387907204
Varsome	rs387907204
LitVar	rs387907204
Map	rs387907204
PheGenI	rs387907204
Biobank	rs387907204
1000 genomes	rs387907204
hgdp	rs387907204
ensembl	rs387907204
geneview	rs387907204
scholar	rs387907204
google	rs387907204
pharmgkb	rs387907204
gwascentral	rs387907204
openSNP	rs387907204
23andMe	rs387907204
SNPshot	rs387907204
SNPdbe	rs387907204
MSV3d	rs387907204
GWAS Ctlg	rs387907204

Max Magnitude

0

ClinVar
Risk	rs387907204(T;T)
Alt	rs387907204(T;T)
Reference	Rs387907204(C;C)
Significance	Other
Disease	Neural tube defects
Variation	info
Gene	FUZ
CLNDBN	Neural tube defects, susceptibility to
Reversed	1
HGVS	NC_000019.9:g.50315990G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024613.6,