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rs1064793120

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome8
Position38424693
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1064793120
dbSNP (old)rs1064793120
ClinGenrs1064793120
ebirs1064793120
HLIrs1064793120
Exacrs1064793120
Gnomadrs1064793120
Varsomers1064793120
Maprs1064793120
PheGenIrs1064793120
Biobankrs1064793120
1000 genomesrs1064793120
hgdprs1064793120
ensemblrs1064793120
gopubmedrs1064793120
geneviewrs1064793120
scholarrs1064793120
googlers1064793120
pharmgkbrs1064793120
gwascentralrs1064793120
openSNPrs1064793120
23andMers1064793120
23andMe allrs1064793120
SNPshotrs1064793120
SNPdbers1064793120
MSV3drs1064793120
GWAS Ctlgrs1064793120
Max Magnitude0
ClinVar
Risk rs1064793120(T;T)
Alt rs1064793120(T;T)
Reference Rs1064793120(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGFR1
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.38282211G>A
CLNSRC
CLNACC RCV000481168.1,