Have questions? Visit https://www.reddit.com/r/SNPedia

rs727502860

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs727502860(-;-)
Make rs727502860(-;C)
Make rs727502860(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position240093503
GeneFMN2
is asnp
is mentioned by
dbSNPrs727502860
ebirs727502860
HLIrs727502860
Exacrs727502860
Varsomers727502860
Maprs727502860
PheGenIrs727502860
hapmaprs727502860
1000 genomesrs727502860
hgdprs727502860
ensemblrs727502860
gopubmedrs727502860
geneviewrs727502860
scholarrs727502860
googlers727502860
pharmgkbrs727502860
gwascentralrs727502860
openSNPrs727502860
23andMers727502860
23andMe allrs727502860
SNP Nexus

SNPshotrs727502860
SNPdbers727502860
MSV3drs727502860
GWAS Ctlgrs727502860
Max Magnitude0
ClinVar
Risk rs727502860(C;C)
Alt rs727502860(C;C)
Reference rs727502860(;)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene FMN2
CLNDBN Mental retardation, autosomal recessive 47
Reversed 0
HGVS NC_000001.10:g.240256803dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000150035.2,