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rs1057517955

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517955(A;A)
Make rs1057517955(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position53199128
GeneKDM5C, MIR6894
is asnp
is mentioned by
dbSNPrs1057517955
dbSNP (old)rs1057517955
ClinGenrs1057517955
ebirs1057517955
HLIrs1057517955
Exacrs1057517955
Gnomadrs1057517955
Varsomers1057517955
Maprs1057517955
PheGenIrs1057517955
Biobankrs1057517955
1000 genomesrs1057517955
hgdprs1057517955
ensemblrs1057517955
gopubmedrs1057517955
geneviewrs1057517955
scholarrs1057517955
googlers1057517955
pharmgkbrs1057517955
gwascentralrs1057517955
openSNPrs1057517955
23andMers1057517955
23andMe allrs1057517955
SNPshotrs1057517955
SNPdbers1057517955
MSV3drs1057517955
GWAS Ctlgrs1057517955
Max Magnitude0
ClinVar
Risk rs1057517955(A;A)
Alt rs1057517955(A;A)
Reference Rs1057517955(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KDM5C MIR6894
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53228310C>T
CLNSRC
CLNACC RCV000413218.1,