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rs1057520697

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520697(G;T)
Make rs1057520697(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position13820500
GeneDNAH5
is asnp
is mentioned by
dbSNPrs1057520697
dbSNP (old)rs1057520697
ClinGenrs1057520697
ebirs1057520697
HLIrs1057520697
Exacrs1057520697
Gnomadrs1057520697
Varsomers1057520697
Maprs1057520697
PheGenIrs1057520697
Biobankrs1057520697
1000 genomesrs1057520697
hgdprs1057520697
ensemblrs1057520697
gopubmedrs1057520697
geneviewrs1057520697
scholarrs1057520697
googlers1057520697
pharmgkbrs1057520697
gwascentralrs1057520697
openSNPrs1057520697
23andMers1057520697
23andMe allrs1057520697
SNPshotrs1057520697
SNPdbers1057520697
MSV3drs1057520697
GWAS Ctlgrs1057520697
Max Magnitude0
ClinVar
Risk rs1057520697(T;T)
Alt rs1057520697(T;T)
Reference Rs1057520697(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DNAH5
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.13820609C>A
CLNSRC
CLNACC RCV000421666.1,