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rs77543610

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs77543610(C;C)
Make rs77543610(C;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position121520160
GeneFGFR2
is asnp
is mentioned by
dbSNPrs77543610
ebirs77543610
HLIrs77543610
Exacrs77543610
Varsomers77543610
Maprs77543610
PheGenIrs77543610
hapmaprs77543610
1000 genomesrs77543610
hgdprs77543610
ensemblrs77543610
gopubmedrs77543610
geneviewrs77543610
scholarrs77543610
googlers77543610
pharmgkbrs77543610
gwascentralrs77543610
openSNPrs77543610
23andMers77543610
23andMe allrs77543610
SNP Nexus

SNPshotrs77543610
SNPdbers77543610
MSV3drs77543610
GWAS Ctlgrs77543610
Max Magnitude0
OMIM176943
Desc
Variant0011
Relatedalso
ClinVar
Risk rs77543610(C;C)
Alt rs77543610(C;C)
Reference rs77543610(G;G)
Significance Pathogenic
Disease Acrocephalosyndactyly type I
Variation info
Gene FGFR2
CLNDBN Acrocephalosyndactyly type I
Reversed 0
HGVS NC_000010.10:g.123279674G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014193.24,