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rs1060499810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499810(A;G)
Make rs1060499810(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position35805671
GeneLHFPL5
is asnp
is mentioned by
dbSNPrs1060499810
dbSNP (old)rs1060499810
ClinGenrs1060499810
ebirs1060499810
HLIrs1060499810
Exacrs1060499810
Gnomadrs1060499810
Varsomers1060499810
LitVarrs1060499810
Maprs1060499810
PheGenIrs1060499810
Biobankrs1060499810
1000 genomesrs1060499810
hgdprs1060499810
ensemblrs1060499810
gopubmedrs1060499810
geneviewrs1060499810
scholarrs1060499810
googlers1060499810
pharmgkbrs1060499810
gwascentralrs1060499810
openSNPrs1060499810
23andMers1060499810
23andMe allrs1060499810
SNPshotrs1060499810
SNPdbers1060499810
MSV3drs1060499810
GWAS Ctlgrs1060499810
Max Magnitude0
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,