Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057519791

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519791(C;G)
Make rs1057519791(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121518810
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057519791
dbSNP (old)rs1057519791
ClinGenrs1057519791
ebirs1057519791
HLIrs1057519791
Exacrs1057519791
Gnomadrs1057519791
Varsomers1057519791
Maprs1057519791
PheGenIrs1057519791
Biobankrs1057519791
1000 genomesrs1057519791
hgdprs1057519791
ensemblrs1057519791
gopubmedrs1057519791
geneviewrs1057519791
scholarrs1057519791
googlers1057519791
pharmgkbrs1057519791
gwascentralrs1057519791
openSNPrs1057519791
23andMers1057519791
23andMe allrs1057519791
SNPshotrs1057519791
SNPdbers1057519791
MSV3drs1057519791
GWAS Ctlgrs1057519791
Max Magnitude0
ClinVar
Risk rs1057519791(G;G)
Alt rs1057519791(G;G)
Reference Rs1057519791(C;C)
Significance Probable-Pathogenic
Disease Squamous cell carcinoma of lung
Variation info
Gene FGFR2
CLNDBN Squamous cell carcinoma of lung
Reversed 1
HGVS NC_000010.10:g.123278324G>C
CLNSRC
CLNACC RCV000437269.1,