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rs575017579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs575017579(A;A)
Make rs575017579(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position13840968
GeneDNAH5
is asnp
is mentioned by
dbSNPrs575017579
dbSNP (classic)rs575017579
ClinGenrs575017579
ebirs575017579
HLIrs575017579
Exacrs575017579
Gnomadrs575017579
Varsomers575017579
LitVarrs575017579
Maprs575017579
PheGenIrs575017579
Biobankrs575017579
1000 genomesrs575017579
hgdprs575017579
ensemblrs575017579
geneviewrs575017579
scholarrs575017579
googlers575017579
pharmgkbrs575017579
gwascentralrs575017579
openSNPrs575017579
23andMers575017579
SNPshotrs575017579
SNPdbers575017579
MSV3drs575017579
GWAS Ctlgrs575017579
Max Magnitude0
ClinVar
Risk rs575017579(A;A) rs575017579(C;C)
Alt rs575017579(A;A) rs575017579(C;C)
Reference Rs575017579(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DNAH5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.13841077G>A
CLNSRC
CLNACC RCV000494045.1,