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rs750797779

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs750797779(A;A)
Make rs750797779(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position36006809
GeneSYNE4
is asnp
is mentioned by
dbSNPrs750797779
dbSNP (old)rs750797779
ClinGenrs750797779
ebirs750797779
HLIrs750797779
Exacrs750797779
Gnomadrs750797779
Varsomers750797779
Maprs750797779
PheGenIrs750797779
Biobankrs750797779
1000 genomesrs750797779
hgdprs750797779
ensemblrs750797779
gopubmedrs750797779
geneviewrs750797779
scholarrs750797779
googlers750797779
pharmgkbrs750797779
gwascentralrs750797779
openSNPrs750797779
23andMers750797779
23andMe allrs750797779
SNP Nexus

SNPshotrs750797779
SNPdbers750797779
MSV3drs750797779
GWAS Ctlgrs750797779
Max Magnitude0
ClinVar
Risk rs750797779(A;A)
Alt rs750797779(A;A)
Reference Rs750797779(G;G)
Significance Probable-Pathogenic
Disease Nonsyndromic hearing loss and deafness
Variation info
Gene SYNE4
CLNDBN Nonsyndromic hearing loss and deafness
Reversed 0
HGVS NC_000019.9:g.36497711G>A
CLNSRC
CLNACC RCV000213729.1,