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rs1057519036

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519036(G;G)
Make rs1057519036(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position121520092
GeneFGFR2
is asnp
is mentioned by
dbSNPrs1057519036
dbSNP (classic)rs1057519036
ClinGenrs1057519036
ebirs1057519036
HLIrs1057519036
Exacrs1057519036
Gnomadrs1057519036
Varsomers1057519036
LitVarrs1057519036
Maprs1057519036
PheGenIrs1057519036
Biobankrs1057519036
1000 genomesrs1057519036
hgdprs1057519036
ensemblrs1057519036
geneviewrs1057519036
scholarrs1057519036
googlers1057519036
pharmgkbrs1057519036
gwascentralrs1057519036
openSNPrs1057519036
23andMers1057519036
23andMe allrs1057519036
SNPshotrs1057519036
SNPdbers1057519036
MSV3drs1057519036
GWAS Ctlgrs1057519036
Max Magnitude0
ClinVar
Risk rs1057519036(G;G)
Alt rs1057519036(G;G)
Reference Rs1057519036(T;T)
Significance Pathogenic
Disease Crouzon syndrome
Variation info
Gene FGFR2
CLNDBN Crouzon syndrome
Reversed 1
HGVS NC_000010.10:g.123279606A>C
CLNSRC
CLNACC RCV000415486.1,