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rs1064796452

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome10
Position121515262
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1064796452
dbSNP (old)rs1064796452
ClinGenrs1064796452
ebirs1064796452
HLIrs1064796452
Exacrs1064796452
Gnomadrs1064796452
Varsomers1064796452
Maprs1064796452
PheGenIrs1064796452
Biobankrs1064796452
1000 genomesrs1064796452
hgdprs1064796452
ensemblrs1064796452
gopubmedrs1064796452
geneviewrs1064796452
scholarrs1064796452
googlers1064796452
pharmgkbrs1064796452
gwascentralrs1064796452
openSNPrs1064796452
23andMers1064796452
23andMe allrs1064796452
SNPshotrs1064796452
SNPdbers1064796452
MSV3drs1064796452
GWAS Ctlgrs1064796452
Max Magnitude0
ClinVar
Risk rs1064796452(G;G)
Alt rs1064796452(G;G)
Reference Rs1064796452(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGFR2
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.123274776T>C
CLNSRC
CLNACC RCV000482209.1,