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rs1057520767

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520767(C;C)
Make rs1057520767(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position92297959
GeneGLMN, RPAP2
is asnp
is mentioned by
dbSNPrs1057520767
dbSNP (old)rs1057520767
ClinGenrs1057520767
ebirs1057520767
HLIrs1057520767
Exacrs1057520767
Gnomadrs1057520767
Varsomers1057520767
LitVarrs1057520767
Maprs1057520767
PheGenIrs1057520767
Biobankrs1057520767
1000 genomesrs1057520767
hgdprs1057520767
ensemblrs1057520767
gopubmedrs1057520767
geneviewrs1057520767
scholarrs1057520767
googlers1057520767
pharmgkbrs1057520767
gwascentralrs1057520767
openSNPrs1057520767
23andMers1057520767
23andMe allrs1057520767
SNPshotrs1057520767
SNPdbers1057520767
MSV3drs1057520767
GWAS Ctlgrs1057520767
Max Magnitude0
ClinVar
Risk rs1057520767(C;C)
Alt rs1057520767(C;C)
Reference Rs1057520767(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene GLMN RPAP2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.92763516A>G
CLNSRC
CLNACC RCV000427751.1,