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rs1057521130

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521130(A;A)
Make rs1057521130(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position18787514
GeneCOMP
is asnp
is mentioned by
dbSNPrs1057521130
dbSNP (old)rs1057521130
ClinGenrs1057521130
ebirs1057521130
HLIrs1057521130
Exacrs1057521130
Gnomadrs1057521130
Varsomers1057521130
Maprs1057521130
PheGenIrs1057521130
Biobankrs1057521130
1000 genomesrs1057521130
hgdprs1057521130
ensemblrs1057521130
gopubmedrs1057521130
geneviewrs1057521130
scholarrs1057521130
googlers1057521130
pharmgkbrs1057521130
gwascentralrs1057521130
openSNPrs1057521130
23andMers1057521130
23andMe allrs1057521130
SNPshotrs1057521130
SNPdbers1057521130
MSV3drs1057521130
GWAS Ctlgrs1057521130
Max Magnitude0
ClinVar
Risk rs1057521130(A;A)
Alt rs1057521130(A;A)
Reference Rs1057521130(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COMP
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.18898323C>T
CLNSRC
CLNACC RCV000433591.1,