rs10510837

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common on affy axiom data

Make rs10510837(A;A)

Make rs10510837(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

60304113

Gene

FHIT

is a	snp
is	mentioned by
dbSNP	rs10510837
dbSNP (classic)	rs10510837
ClinGen	rs10510837
ebi	rs10510837
HLI	rs10510837
Exac	rs10510837
Gnomad	rs10510837
Varsome	rs10510837
LitVar	rs10510837
Map	rs10510837
PheGenI	rs10510837
Biobank	rs10510837
1000 genomes	rs10510837
hgdp	rs10510837
ensembl	rs10510837
geneview	rs10510837
scholar	rs10510837
google	rs10510837
pharmgkb	rs10510837
gwascentral	rs10510837
openSNP	rs10510837
23andMe	rs10510837
SNPshot	rs10510837
SNPdbe	rs10510837
MSV3d	rs10510837
GWAS Ctlg	rs10510837

GMAF

0.09688

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 21182207]
Trait
Title	Variants in several genomic regions associated with Asperger disorder
Risk Allele
P-val	0.000004
Odds Ratio	None None