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rs1064793123

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome8
Position38421859
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1064793123
dbSNP (old)rs1064793123
ClinGenrs1064793123
ebirs1064793123
HLIrs1064793123
Exacrs1064793123
Gnomadrs1064793123
Varsomers1064793123
Maprs1064793123
PheGenIrs1064793123
Biobankrs1064793123
1000 genomesrs1064793123
hgdprs1064793123
ensemblrs1064793123
gopubmedrs1064793123
geneviewrs1064793123
scholarrs1064793123
googlers1064793123
pharmgkbrs1064793123
gwascentralrs1064793123
openSNPrs1064793123
23andMers1064793123
23andMe allrs1064793123
SNPshotrs1064793123
SNPdbers1064793123
MSV3drs1064793123
GWAS Ctlgrs1064793123
Max Magnitude0
ClinVar
Risk rs1064793123(T;T)
Alt rs1064793123(T;T)
Reference Rs1064793123(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGFR1
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.38279377G>A
CLNSRC
CLNACC RCV000480479.1,