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rs727502861

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727502861(-;-)
Make rs727502861(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position240207327
GeneFMN2
is asnp
is mentioned by
dbSNPrs727502861
ebirs727502861
HLIrs727502861
Exacrs727502861
Varsomers727502861
Maprs727502861
PheGenIrs727502861
hapmaprs727502861
1000 genomesrs727502861
hgdprs727502861
ensemblrs727502861
gopubmedrs727502861
geneviewrs727502861
scholarrs727502861
googlers727502861
pharmgkbrs727502861
gwascentralrs727502861
openSNPrs727502861
23andMers727502861
23andMe allrs727502861
SNP Nexus

SNPshotrs727502861
SNPdbers727502861
MSV3drs727502861
GWAS Ctlgrs727502861
Max Magnitude0
ClinVar
Risk rs727502861(;)
Alt rs727502861(;)
Reference rs727502861(A;A)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene FMN2
CLNDBN Mental retardation, autosomal recessive 47
Reversed 0
HGVS NC_000001.10:g.240370627delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000150036.4,