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rs869312227

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312227(A;A)
Make rs869312227(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101397981
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312227
ebirs869312227
HLIrs869312227
Exacrs869312227
Varsomers869312227
Maprs869312227
PheGenIrs869312227
hapmaprs869312227
1000 genomesrs869312227
hgdprs869312227
ensemblrs869312227
gopubmedrs869312227
geneviewrs869312227
scholarrs869312227
googlers869312227
pharmgkbrs869312227
gwascentralrs869312227
openSNPrs869312227
23andMers869312227
23andMe allrs869312227
SNP Nexus

SNPshotrs869312227
SNPdbers869312227
MSV3drs869312227
GWAS Ctlgrs869312227
Max Magnitude0
ClinVar
Risk rs869312227(A;A)
Alt rs869312227(A;A)
Reference rs869312227(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100652969C>T
CLNSRC
CLNACC RCV000236260.1,