rs878853235

Orientation

plus

Stabilized

plus

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

Make rs878853235(A;G)

Make rs878853235(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

77156889

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs878853235
dbSNP (classic)	rs878853235
ClinGen	rs878853235
ebi	rs878853235
HLI	rs878853235
Exac	rs878853235
Gnomad	rs878853235
Varsome	rs878853235
LitVar	rs878853235
Map	rs878853235
PheGenI	rs878853235
Biobank	rs878853235
1000 genomes	rs878853235
hgdp	rs878853235
ensembl	rs878853235
geneview	rs878853235
scholar	rs878853235
google	rs878853235
pharmgkb	rs878853235
gwascentral	rs878853235
openSNP	rs878853235
23andMe	rs878853235
SNPshot	rs878853235
SNPdbe	rs878853235
MSV3d	rs878853235
GWAS Ctlg	rs878853235

Max Magnitude

0

ClinVar
Risk	rs878853235(G;G)
Alt	rs878853235(G;G)
Reference	Rs878853235(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO7A
CLNDBN	Deafness, autosomal recessive 2
Reversed	0
HGVS	NC_000011.9:g.76867935A>G
CLNSRC
CLNACC	RCV000225019.1,