rs8077577

Orientation

plus

Stabilized

plus

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

Make rs8077577(C;T)

Make rs8077577(T;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

18161416

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs8077577
dbSNP (classic)	rs8077577
ClinGen	rs8077577
ebi	rs8077577
HLI	rs8077577
Exac	rs8077577
Gnomad	rs8077577
Varsome	rs8077577
LitVar	rs8077577
Map	rs8077577
PheGenI	rs8077577
Biobank	rs8077577
1000 genomes	rs8077577
hgdp	rs8077577
ensembl	rs8077577
geneview	rs8077577
scholar	rs8077577
google	rs8077577
pharmgkb	rs8077577
gwascentral	rs8077577
openSNP	rs8077577
23andMe	rs8077577
SNPshot	rs8077577
SNPdbe	rs8077577
MSV3d	rs8077577
GWAS Ctlg	rs8077577

Max Magnitude

0

GWAS snp
PMID	[PMID 23251661]
Trait	Obesity-related traits
Title	Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele	A
P-val	4E-6
Odds Ratio	.03 [NR] ng/mL increase

ClinVar
Risk	rs8077577(T;T)
Alt	rs8077577(T;T)
Reference	Rs8077577(C;C)
Significance	Probable-non-pathogenic
Disease	not specified Nonsyndromic Hearing Loss
Variation	info
Gene	MYO15A
CLNDBN	not specified Nonsyndromic Hearing Loss, Recessive
Reversed	0
HGVS	NC_000017.10:g.18064730C>T
CLNSRC	ClinVar
CLNACC	RCV000038998.4, RCV000274944.1,