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rs1057519232

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519232(-;T)
Make rs1057519232(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position23417092
GeneCOG7
is asnp
is mentioned by
dbSNPrs1057519232
dbSNP (classic)rs1057519232
ClinGenrs1057519232
ebirs1057519232
HLIrs1057519232
Exacrs1057519232
Gnomadrs1057519232
Varsomers1057519232
LitVarrs1057519232
Maprs1057519232
PheGenIrs1057519232
Biobankrs1057519232
1000 genomesrs1057519232
hgdprs1057519232
ensemblrs1057519232
geneviewrs1057519232
scholarrs1057519232
googlers1057519232
pharmgkbrs1057519232
gwascentralrs1057519232
openSNPrs1057519232
23andMers1057519232
23andMe allrs1057519232
SNPshotrs1057519232
SNPdbers1057519232
MSV3drs1057519232
GWAS Ctlgrs1057519232
Max Magnitude0
ClinVar
Risk rs1057519232(T;T)
Alt rs1057519232(T;T)
Reference Rs1057519232(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COG7
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.23428413_23428414insA
CLNSRC
CLNACC RCV000415987.1,