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rs1057518014

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCCTC;CCCTC) 0 common in clinvar
Make rs1057518014(-;-)
Make rs1057518014(-;CCCTC)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position143817103
GenePUF60, SCRIB
is asnp
is mentioned by
dbSNPrs1057518014
dbSNP (classic)rs1057518014
ClinGenrs1057518014
ebirs1057518014
HLIrs1057518014
Exacrs1057518014
Gnomadrs1057518014
Varsomers1057518014
LitVarrs1057518014
Maprs1057518014
PheGenIrs1057518014
Biobankrs1057518014
1000 genomesrs1057518014
hgdprs1057518014
ensemblrs1057518014
geneviewrs1057518014
scholarrs1057518014
googlers1057518014
pharmgkbrs1057518014
gwascentralrs1057518014
openSNPrs1057518014
23andMers1057518014
23andMe allrs1057518014
SNPshotrs1057518014
SNPdbers1057518014
MSV3drs1057518014
GWAS Ctlgrs1057518014
Max Magnitude0
ClinVar
Risk rs1057518014(-;-)
Alt rs1057518014(-;-)
Reference Rs1057518014(CCCTC;CCCTC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PUF60 SCRIB
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.144899273_144899277delGAGGG
CLNSRC
CLNACC RCV000413995.1,