rs878853237

Orientation

plus

Stabilized

plus

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

Make rs878853237(C;C)

Make rs878853237(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

77142719

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs878853237
dbSNP (classic)	rs878853237
ClinGen	rs878853237
ebi	rs878853237
HLI	rs878853237
Exac	rs878853237
Gnomad	rs878853237
Varsome	rs878853237
LitVar	rs878853237
Map	rs878853237
PheGenI	rs878853237
Biobank	rs878853237
1000 genomes	rs878853237
hgdp	rs878853237
ensembl	rs878853237
geneview	rs878853237
scholar	rs878853237
google	rs878853237
pharmgkb	rs878853237
gwascentral	rs878853237
openSNP	rs878853237
23andMe	rs878853237
SNPshot	rs878853237
SNPdbe	rs878853237
MSV3d	rs878853237
GWAS Ctlg	rs878853237

Max Magnitude

0

ClinVar
Risk	rs878853237(C;C)
Alt	rs878853237(C;C)
Reference	Rs878853237(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO7A
CLNDBN	Deafness, autosomal recessive 2
Reversed	0
HGVS	NC_000011.9:g.76853765T>C
CLNSRC
CLNACC	RCV000225048.1,