rs387906699

Orientation

plus

Stabilized

plus

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

Make rs387906699(A;A)

Make rs387906699(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77174831

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs387906699
dbSNP (classic)	rs387906699
ClinGen	rs387906699
ebi	rs387906699
HLI	rs387906699
Exac	rs387906699
Gnomad	rs387906699
Varsome	rs387906699
LitVar	rs387906699
Map	rs387906699
PheGenI	rs387906699
Biobank	rs387906699
1000 genomes	rs387906699
hgdp	rs387906699
ensembl	rs387906699
geneview	rs387906699
scholar	rs387906699
google	rs387906699
pharmgkb	rs387906699
gwascentral	rs387906699
openSNP	rs387906699
23andMe	rs387906699
SNPshot	rs387906699
SNPdbe	rs387906699
MSV3d	rs387906699
GWAS Ctlg	rs387906699

Max Magnitude

0

ClinVar
Risk	rs387906699(A;A)
Alt	rs387906699(A;A)
Reference	Rs387906699(G;G)
Significance	Pathogenic
Disease	Deafness not specified
Variation	info
Gene	MYO7A
CLNDBN	Deafness, autosomal dominant 11 not specified
Reversed	0
HGVS	NC_000011.9:g.76885877G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022816.17, RCV000151492.2,