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rs1057518481

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518481(A;T)
Make rs1057518481(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position38414903
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1057518481
dbSNP (old)rs1057518481
ClinGenrs1057518481
ebirs1057518481
HLIrs1057518481
Exacrs1057518481
Gnomadrs1057518481
Varsomers1057518481
Maprs1057518481
PheGenIrs1057518481
Biobankrs1057518481
1000 genomesrs1057518481
hgdprs1057518481
ensemblrs1057518481
gopubmedrs1057518481
geneviewrs1057518481
scholarrs1057518481
googlers1057518481
pharmgkbrs1057518481
gwascentralrs1057518481
openSNPrs1057518481
23andMers1057518481
23andMe allrs1057518481
SNPshotrs1057518481
SNPdbers1057518481
MSV3drs1057518481
GWAS Ctlgrs1057518481
Max Magnitude0
ClinVar
Risk rs1057518481(T;T)
Alt rs1057518481(T;T)
Reference Rs1057518481(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGFR1
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.38272421T>A
CLNSRC
CLNACC RCV000413313.1,