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rs1057523840

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057523840(A;G)
Make rs1057523840(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position160282588
GeneIFT80
is asnp
is mentioned by
dbSNPrs1057523840
dbSNP (old)rs1057523840
ClinGenrs1057523840
ebirs1057523840
HLIrs1057523840
Exacrs1057523840
Gnomadrs1057523840
Varsomers1057523840
Maprs1057523840
PheGenIrs1057523840
Biobankrs1057523840
1000 genomesrs1057523840
hgdprs1057523840
ensemblrs1057523840
gopubmedrs1057523840
geneviewrs1057523840
scholarrs1057523840
googlers1057523840
pharmgkbrs1057523840
gwascentralrs1057523840
openSNPrs1057523840
23andMers1057523840
23andMe allrs1057523840
SNPshotrs1057523840
SNPdbers1057523840
MSV3drs1057523840
GWAS Ctlgrs1057523840
Max Magnitude0
ClinVar
Risk rs1057523840(G;G)
Alt rs1057523840(G;G)
Reference Rs1057523840(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IFT80
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.160000376T>C
CLNSRC
CLNACC RCV000418165.1,