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rs121918509

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918509(A;A)
Make rs121918509(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position121488095
GeneFGFR2
is asnp
is mentioned by
dbSNPrs121918509
ebirs121918509
HLIrs121918509
Exacrs121918509
Varsomers121918509
Maprs121918509
PheGenIrs121918509
hapmaprs121918509
1000 genomesrs121918509
hgdprs121918509
ensemblrs121918509
gopubmedrs121918509
geneviewrs121918509
scholarrs121918509
googlers121918509
pharmgkbrs121918509
gwascentralrs121918509
openSNPrs121918509
23andMers121918509
23andMe allrs121918509
SNP Nexus

SNPshotrs121918509
SNPdbers121918509
MSV3drs121918509
GWAS Ctlgrs121918509
Max Magnitude0
OMIM176943
Desc
Variant0037
Relatedalso
ClinVar
Risk rs121918509(A;A)
Alt rs121918509(A;A)
Reference rs121918509(G;G)
Significance Pathogenic
Disease Levy-Hollister syndrome
Variation info
Gene FGFR2
CLNDBN Levy-Hollister syndrome
Reversed 1
HGVS NC_000010.10:g.123247609C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014224.23,