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rs1057524546

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524546(G;T)
Make rs1057524546(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position38414265
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1057524546
dbSNP (old)rs1057524546
ClinGenrs1057524546
ebirs1057524546
HLIrs1057524546
Exacrs1057524546
Gnomadrs1057524546
Varsomers1057524546
Maprs1057524546
PheGenIrs1057524546
Biobankrs1057524546
1000 genomesrs1057524546
hgdprs1057524546
ensemblrs1057524546
gopubmedrs1057524546
geneviewrs1057524546
scholarrs1057524546
googlers1057524546
pharmgkbrs1057524546
gwascentralrs1057524546
openSNPrs1057524546
23andMers1057524546
23andMe allrs1057524546
SNPshotrs1057524546
SNPdbers1057524546
MSV3drs1057524546
GWAS Ctlgrs1057524546
Max Magnitude0
ClinVar
Risk rs1057524546(T;T)
Alt rs1057524546(T;T)
Reference Rs1057524546(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGFR1
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.38271783C>A
CLNSRC
CLNACC RCV000430948.1,