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rs1057520198

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520198(C;C)
Make rs1057520198(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position53220843
GeneKDM5C
is asnp
is mentioned by
dbSNPrs1057520198
dbSNP (classic)rs1057520198
ClinGenrs1057520198
ebirs1057520198
HLIrs1057520198
Exacrs1057520198
Gnomadrs1057520198
Varsomers1057520198
LitVarrs1057520198
Maprs1057520198
PheGenIrs1057520198
Biobankrs1057520198
1000 genomesrs1057520198
hgdprs1057520198
ensemblrs1057520198
geneviewrs1057520198
scholarrs1057520198
googlers1057520198
pharmgkbrs1057520198
gwascentralrs1057520198
openSNPrs1057520198
23andMers1057520198
23andMe allrs1057520198
SNPshotrs1057520198
SNPdbers1057520198
MSV3drs1057520198
GWAS Ctlgrs1057520198
Max Magnitude0
ClinVar
Risk rs1057520198(C;C)
Alt rs1057520198(C;C)
Reference Rs1057520198(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KDM5C
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53250025A>G
CLNSRC
CLNACC RCV000420674.1,