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rs761622153

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761622153(A;A)
Make rs761622153(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position13841112
GeneDNAH5
is asnp
is mentioned by
dbSNPrs761622153
dbSNP (classic)rs761622153
ClinGenrs761622153
ebirs761622153
HLIrs761622153
Exacrs761622153
Gnomadrs761622153
Varsomers761622153
LitVarrs761622153
Maprs761622153
PheGenIrs761622153
Biobankrs761622153
1000 genomesrs761622153
hgdprs761622153
ensemblrs761622153
geneviewrs761622153
scholarrs761622153
googlers761622153
pharmgkbrs761622153
gwascentralrs761622153
openSNPrs761622153
23andMers761622153
SNPshotrs761622153
SNPdbers761622153
MSV3drs761622153
GWAS Ctlgrs761622153
Max Magnitude0
ClinVar
Risk rs761622153(A;A)
Alt rs761622153(A;A)
Reference Rs761622153(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNAH5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.13841221G>A
CLNSRC
CLNACC RCV000413667.1,