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rs1057520746

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520746(C;T)
Make rs1057520746(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position92837463
GeneFAM69A, RPL5, SNORD21
is asnp
is mentioned by
dbSNPrs1057520746
dbSNP (old)rs1057520746
ClinGenrs1057520746
ebirs1057520746
HLIrs1057520746
Exacrs1057520746
Gnomadrs1057520746
Varsomers1057520746
Maprs1057520746
PheGenIrs1057520746
Biobankrs1057520746
1000 genomesrs1057520746
hgdprs1057520746
ensemblrs1057520746
gopubmedrs1057520746
geneviewrs1057520746
scholarrs1057520746
googlers1057520746
pharmgkbrs1057520746
gwascentralrs1057520746
openSNPrs1057520746
23andMers1057520746
23andMe allrs1057520746
SNPshotrs1057520746
SNPdbers1057520746
MSV3drs1057520746
GWAS Ctlgrs1057520746
Max Magnitude0
ClinVar
Risk rs1057520746(T;T)
Alt rs1057520746(T;T)
Reference Rs1057520746(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL5 FAM69A SNORD21
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.93303020C>T
CLNSRC
CLNACC RCV000441812.1,