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rs1057517926

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517926(A;A)
Make rs1057517926(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position13728665
GeneFAR1
is asnp
is mentioned by
dbSNPrs1057517926
dbSNP (old)rs1057517926
ClinGenrs1057517926
ebirs1057517926
HLIrs1057517926
Exacrs1057517926
Gnomadrs1057517926
Varsomers1057517926
LitVarrs1057517926
Maprs1057517926
PheGenIrs1057517926
Biobankrs1057517926
1000 genomesrs1057517926
hgdprs1057517926
ensemblrs1057517926
gopubmedrs1057517926
geneviewrs1057517926
scholarrs1057517926
googlers1057517926
pharmgkbrs1057517926
gwascentralrs1057517926
openSNPrs1057517926
23andMers1057517926
23andMe allrs1057517926
SNPshotrs1057517926
SNPdbers1057517926
MSV3drs1057517926
GWAS Ctlgrs1057517926
Max Magnitude0
ClinVar
Risk rs1057517926(A;A) rs1057517926(T;T)
Alt rs1057517926(A;A) rs1057517926(T;T)
Reference Rs1057517926(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene FAR1
CLNDBN not provided not specified
Reversed 0
HGVS NC_000011.9:g.13750212G>A; NC_000011.9:g.13750212G>T
CLNSRC
CLNACC RCV000413132.1, RCV000489959.1,