rs139365610

Orientation

plus

Stabilized

plus

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

Make rs139365610(C;T)

Make rs139365610(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

49807348

Gene	AP2A1, FUZ, LOC105372435

is a	snp
is	mentioned by
dbSNP	rs139365610
dbSNP (classic)	rs139365610
ClinGen	rs139365610
ebi	rs139365610
HLI	rs139365610
Exac	rs139365610
Gnomad	rs139365610
Varsome	rs139365610
LitVar	rs139365610
Map	rs139365610
PheGenI	rs139365610
Biobank	rs139365610
1000 genomes	rs139365610
hgdp	rs139365610
ensembl	rs139365610
geneview	rs139365610
scholar	rs139365610
google	rs139365610
pharmgkb	rs139365610
gwascentral	rs139365610
openSNP	rs139365610
23andMe	rs139365610
SNPshot	rs139365610
SNPdbe	rs139365610
MSV3d	rs139365610
GWAS Ctlg	rs139365610

Max Magnitude

0

ClinVar
Risk	rs139365610(A;A) rs139365610(T;T)
Alt	rs139365610(A;A) rs139365610(T;T)
Reference	Rs139365610(C;C)
Significance	Other
Disease	Neural tube defects
Variation	info
Gene	FUZ AP2A1
CLNDBN	Neural tube defects, susceptibility to
Reversed	0
HGVS	NC_000019.9:g.50310605C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024614.4,