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rs1057519105

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519105(A;T)
Make rs1057519105(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position21773907
GeneDNAH11
is asnp
is mentioned by
dbSNPrs1057519105
dbSNP (old)rs1057519105
ClinGenrs1057519105
ebirs1057519105
HLIrs1057519105
Exacrs1057519105
Gnomadrs1057519105
Varsomers1057519105
Maprs1057519105
PheGenIrs1057519105
Biobankrs1057519105
1000 genomesrs1057519105
hgdprs1057519105
ensemblrs1057519105
gopubmedrs1057519105
geneviewrs1057519105
scholarrs1057519105
googlers1057519105
pharmgkbrs1057519105
gwascentralrs1057519105
openSNPrs1057519105
23andMers1057519105
23andMe allrs1057519105
SNPshotrs1057519105
SNPdbers1057519105
MSV3drs1057519105
GWAS Ctlgrs1057519105
Max Magnitude0
ClinVar
Risk rs1057519105(T;T)
Alt rs1057519105(T;T)
Reference Rs1057519105(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNAH11
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.21813525A>T
CLNSRC
CLNACC RCV000415908.1,