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

rs1064796413

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome10
Position121488052
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1064796413
dbSNP (old)rs1064796413
ClinGenrs1064796413
ebirs1064796413
HLIrs1064796413
Exacrs1064796413
Gnomadrs1064796413
Varsomers1064796413
Maprs1064796413
PheGenIrs1064796413
Biobankrs1064796413
1000 genomesrs1064796413
hgdprs1064796413
ensemblrs1064796413
gopubmedrs1064796413
geneviewrs1064796413
scholarrs1064796413
googlers1064796413
pharmgkbrs1064796413
gwascentralrs1064796413
openSNPrs1064796413
23andMers1064796413
23andMe allrs1064796413
SNPshotrs1064796413
SNPdbers1064796413
MSV3drs1064796413
GWAS Ctlgrs1064796413
Max Magnitude0
ClinVar
Risk rs1064796413(A;A)
Alt rs1064796413(A;A)
Reference Rs1064796413(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGFR2
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.123247566A>T
CLNSRC
CLNACC RCV000478596.1,