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rs1057518064

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518064(C;G)
Make rs1057518064(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position1562008
GeneIFT140
is asnp
is mentioned by
dbSNPrs1057518064
dbSNP (old)rs1057518064
ClinGenrs1057518064
ebirs1057518064
HLIrs1057518064
Exacrs1057518064
Gnomadrs1057518064
Varsomers1057518064
Maprs1057518064
PheGenIrs1057518064
Biobankrs1057518064
1000 genomesrs1057518064
hgdprs1057518064
ensemblrs1057518064
gopubmedrs1057518064
geneviewrs1057518064
scholarrs1057518064
googlers1057518064
pharmgkbrs1057518064
gwascentralrs1057518064
openSNPrs1057518064
23andMers1057518064
23andMe allrs1057518064
SNPshotrs1057518064
SNPdbers1057518064
MSV3drs1057518064
GWAS Ctlgrs1057518064
Max Magnitude0
ClinVar
Risk rs1057518064(G;G)
Alt rs1057518064(G;G)
Reference Rs1057518064(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IFT140
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.1612009G>C
CLNSRC
CLNACC RCV000413732.1,