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rs1057524366

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524366(A;C)
Make rs1057524366(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position27312684
GeneMPV17
is asnp
is mentioned by
dbSNPrs1057524366
dbSNP (old)rs1057524366
ClinGenrs1057524366
ebirs1057524366
HLIrs1057524366
Exacrs1057524366
Gnomadrs1057524366
Varsomers1057524366
LitVarrs1057524366
Maprs1057524366
PheGenIrs1057524366
Biobankrs1057524366
1000 genomesrs1057524366
hgdprs1057524366
ensemblrs1057524366
gopubmedrs1057524366
geneviewrs1057524366
scholarrs1057524366
googlers1057524366
pharmgkbrs1057524366
gwascentralrs1057524366
openSNPrs1057524366
23andMers1057524366
23andMe allrs1057524366
SNPshotrs1057524366
SNPdbers1057524366
MSV3drs1057524366
GWAS Ctlgrs1057524366
Max Magnitude0
ClinVar
Risk rs1057524366(C;C)
Alt rs1057524366(C;C)
Reference Rs1057524366(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MPV17
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.27535551T>G
CLNSRC
CLNACC RCV000419357.1,