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rs1057521047

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521047(C;C)
Make rs1057521047(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position101407750
GeneGLA, HNRNPH2, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs1057521047
dbSNP (classic)rs1057521047
ClinGenrs1057521047
ebirs1057521047
HLIrs1057521047
Exacrs1057521047
Gnomadrs1057521047
Varsomers1057521047
LitVarrs1057521047
Maprs1057521047
PheGenIrs1057521047
Biobankrs1057521047
1000 genomesrs1057521047
hgdprs1057521047
ensemblrs1057521047
geneviewrs1057521047
scholarrs1057521047
googlers1057521047
pharmgkbrs1057521047
gwascentralrs1057521047
openSNPrs1057521047
23andMers1057521047
SNPshotrs1057521047
SNPdbers1057521047
MSV3drs1057521047
GWAS Ctlgrs1057521047
Max Magnitude0
ClinVar
Risk rs1057521047(C;C)
Alt rs1057521047(C;C)
Reference Rs1057521047(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene HNRNPH2 RPL36A-HNRNPH2 GLA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100662738A>G
CLNSRC
CLNACC RCV000424225.1,