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rs587777012

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777012(C;C)
Make rs587777012(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position59153199
GeneFAM111A
is asnp
is mentioned by
dbSNPrs587777012
ebirs587777012
HLIrs587777012
Exacrs587777012
Varsomers587777012
Maprs587777012
PheGenIrs587777012
hapmaprs587777012
1000 genomesrs587777012
hgdprs587777012
ensemblrs587777012
gopubmedrs587777012
geneviewrs587777012
scholarrs587777012
googlers587777012
pharmgkbrs587777012
gwascentralrs587777012
openSNPrs587777012
23andMers587777012
23andMe allrs587777012
SNP Nexus

SNPshotrs587777012
SNPdbers587777012
MSV3drs587777012
GWAS Ctlgrs587777012
Max Magnitude0
ClinVar
Risk rs587777012(C;C)
Alt rs587777012(C;C)
Reference rs587777012(T;T)
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.58920672T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000050211.3,