rs762352115

Orientation

plus

Stabilized

plus

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

Make rs762352115(A;A)

Make rs762352115(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

69432676

Gene

MARVELD2

is a	snp
is	mentioned by
dbSNP	rs762352115
dbSNP (classic)	rs762352115
ClinGen	rs762352115
ebi	rs762352115
HLI	rs762352115
Exac	rs762352115
Gnomad	rs762352115
Varsome	rs762352115
LitVar	rs762352115
Map	rs762352115
PheGenI	rs762352115
Biobank	rs762352115
1000 genomes	rs762352115
hgdp	rs762352115
ensembl	rs762352115
geneview	rs762352115
scholar	rs762352115
google	rs762352115
pharmgkb	rs762352115
gwascentral	rs762352115
openSNP	rs762352115
23andMe	rs762352115
SNPshot	rs762352115
SNPdbe	rs762352115
MSV3d	rs762352115
GWAS Ctlg	rs762352115

Max Magnitude

0

ClinVar
Risk	rs762352115(A;A)
Alt	rs762352115(A;A)
Reference	Rs762352115(G;G)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	MARVELD2
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000005.9:g.68728503G>A
CLNSRC
CLNACC	RCV000214632.1,