Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518060

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518060(C;C)
Make rs1057518060(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position38414276
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1057518060
dbSNP (old)rs1057518060
ClinGenrs1057518060
ebirs1057518060
HLIrs1057518060
Exacrs1057518060
Gnomadrs1057518060
Varsomers1057518060
Maprs1057518060
PheGenIrs1057518060
Biobankrs1057518060
1000 genomesrs1057518060
hgdprs1057518060
ensemblrs1057518060
gopubmedrs1057518060
geneviewrs1057518060
scholarrs1057518060
googlers1057518060
pharmgkbrs1057518060
gwascentralrs1057518060
openSNPrs1057518060
23andMers1057518060
23andMe allrs1057518060
SNPshotrs1057518060
SNPdbers1057518060
MSV3drs1057518060
GWAS Ctlgrs1057518060
Max Magnitude0
ClinVar
Risk rs1057518060(C;C)
Alt rs1057518060(C;C)
Reference Rs1057518060(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGFR1
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.38271794C>G
CLNSRC
CLNACC RCV000413066.1,