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rs879253720

From SNPedia

Orientationminus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs879253720(-;-)
Make rs879253720(-;AGA)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position121488028
GeneFGFR2
is asnp
is mentioned by
dbSNPrs879253720
ebirs879253720
HLIrs879253720
Exacrs879253720
Varsomers879253720
Maprs879253720
PheGenIrs879253720
hapmaprs879253720
1000 genomesrs879253720
hgdprs879253720
ensemblrs879253720
gopubmedrs879253720
geneviewrs879253720
scholarrs879253720
googlers879253720
pharmgkbrs879253720
gwascentralrs879253720
openSNPrs879253720
23andMers879253720
23andMe allrs879253720
SNP Nexus

SNPshotrs879253720
SNPdbers879253720
MSV3drs879253720
GWAS Ctlgrs879253720
Max Magnitude0
ClinVar
Risk rs879253720(;)
Alt rs879253720(;)
Reference rs879253720(AGA;AGA)
Significance Pathogenic
Disease Levy-Hollister syndrome
Variation info
Gene FGFR2
CLNDBN Levy-Hollister syndrome
Reversed 1
HGVS NC_000010.10:g.123247542_123247544delTCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000014223.17,