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rs397515869

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515869(A;G)
Make rs397515869(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position101397946
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs397515869
ebirs397515869
HLIrs397515869
Exacrs397515869
Varsomers397515869
Maprs397515869
PheGenIrs397515869
hapmaprs397515869
1000 genomesrs397515869
hgdprs397515869
ensemblrs397515869
gopubmedrs397515869
geneviewrs397515869
scholarrs397515869
googlers397515869
pharmgkbrs397515869
gwascentralrs397515869
openSNPrs397515869
23andMers397515869
23andMe allrs397515869
SNP Nexus

SNPshotrs397515869
SNPdbers397515869
MSV3drs397515869
GWAS Ctlgrs397515869
Max Magnitude0
ClinVar
Risk rs397515869(G;G)
Alt rs397515869(G;G)
Reference rs397515869(A;A)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN not specified
Reversed 1
HGVS NC_000023.10:g.100652934T>C
CLNSRC University of Rostock
CLNACC RCV000035301.3,