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rs587777011

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777011(A;A)
Make rs587777011(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position59153374
GeneFAM111A
is asnp
is mentioned by
dbSNPrs587777011
ebirs587777011
HLIrs587777011
Exacrs587777011
Varsomers587777011
Maprs587777011
PheGenIrs587777011
hapmaprs587777011
1000 genomesrs587777011
hgdprs587777011
ensemblrs587777011
gopubmedrs587777011
geneviewrs587777011
scholarrs587777011
googlers587777011
pharmgkbrs587777011
gwascentralrs587777011
openSNPrs587777011
23andMers587777011
23andMe allrs587777011
SNP Nexus

SNPshotrs587777011
SNPdbers587777011
MSV3drs587777011
GWAS Ctlgrs587777011
Max Magnitude0
ClinVar
Risk rs587777011(A;A)
Alt rs587777011(A;A)
Reference rs587777011(G;G)
Significance Other
Disease Kenny-Caffey syndrome type 2
Variation info
Gene FAM111A
CLNDBN Kenny-Caffey syndrome type 2
Reversed 0
HGVS NC_000011.9:g.58920847G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000050209.3,