rs1060499810

Orientation

plus

Stabilized

plus

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

Make rs1060499810(A;G)

Make rs1060499810(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

35805671

Gene

LHFPL5

is a	snp
is	mentioned by
dbSNP	rs1060499810
dbSNP (classic)	rs1060499810
ClinGen	rs1060499810
ebi	rs1060499810
HLI	rs1060499810
Exac	rs1060499810
Gnomad	rs1060499810
Varsome	rs1060499810
LitVar	rs1060499810
Map	rs1060499810
PheGenI	rs1060499810
Biobank	rs1060499810
1000 genomes	rs1060499810
hgdp	rs1060499810
ensembl	rs1060499810
geneview	rs1060499810
scholar	rs1060499810
google	rs1060499810
pharmgkb	rs1060499810
gwascentral	rs1060499810
openSNP	rs1060499810
23andMe	rs1060499810
SNPshot	rs1060499810
SNPdbe	rs1060499810
MSV3d	rs1060499810
GWAS Ctlg	rs1060499810

Max Magnitude

0

ClinVar
Risk	rs1060499810(G;G)
Alt	rs1060499810(G;G)
Reference	Rs1060499810(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	LHFPL5
CLNDBN	Deafness, autosomal recessive 67
Reversed	0
HGVS	NC_000006.11:g.35773448A>G
CLNSRC
CLNACC	RCV000454165.1,