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rs1085307879

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome8
Position38414183
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1085307879
dbSNP (old)rs1085307879
ClinGenrs1085307879
ebirs1085307879
HLIrs1085307879
Exacrs1085307879
Gnomadrs1085307879
Varsomers1085307879
LitVarrs1085307879
Maprs1085307879
PheGenIrs1085307879
Biobankrs1085307879
1000 genomesrs1085307879
hgdprs1085307879
ensemblrs1085307879
gopubmedrs1085307879
geneviewrs1085307879
scholarrs1085307879
googlers1085307879
pharmgkbrs1085307879
gwascentralrs1085307879
openSNPrs1085307879
23andMers1085307879
23andMe allrs1085307879
SNPshotrs1085307879
SNPdbers1085307879
MSV3drs1085307879
GWAS Ctlgrs1085307879
Max Magnitude0
ClinVar
Risk rs1085307879(G;G)
Alt rs1085307879(G;G)
Reference Rs1085307879(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGFR1
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.38271701T>C
CLNSRC
CLNACC RCV000490235.1,