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rs730882244

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730882244(-;-)
Make rs730882244(-;A)
Make rs730882244(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position35077176
GeneFAM177A1
is asnp
is mentioned by
dbSNPrs730882244
ebirs730882244
HLIrs730882244
Exacrs730882244
Varsomers730882244
Maprs730882244
PheGenIrs730882244
hapmaprs730882244
1000 genomesrs730882244
hgdprs730882244
ensemblrs730882244
gopubmedrs730882244
geneviewrs730882244
scholarrs730882244
googlers730882244
pharmgkbrs730882244
gwascentralrs730882244
openSNPrs730882244
23andMers730882244
23andMe allrs730882244
SNP Nexus

SNPshotrs730882244
SNPdbers730882244
MSV3drs730882244
GWAS Ctlgrs730882244
Max Magnitude0
ClinVar
Risk rs730882244(A;A)
Alt rs730882244(A;A)
Reference rs730882244(;)
Significance Probable-Pathogenic
Disease Dolichocephaly Intellectual disability Macrocephaly Mild obesity
Variation info
Gene FAM177A1
CLNDBN Dolichocephaly Intellectual disability Macrocephaly Mild obesity
Reversed 0
HGVS NC_000014.8:g.35546382dupA
CLNSRC King Faisal Specialist Hospital and Research Center
CLNACC RCV000162180.1,