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

rs727502773

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs727502773(-;-)
Make rs727502773(-;AG)
Make rs727502773(AG;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position76179693
GeneSCARB2
is asnp
is mentioned by
dbSNPrs727502773
ebirs727502773
HLIrs727502773
Exacrs727502773
Varsomers727502773
Maprs727502773
PheGenIrs727502773
hapmaprs727502773
1000 genomesrs727502773
hgdprs727502773
ensemblrs727502773
gopubmedrs727502773
geneviewrs727502773
scholarrs727502773
googlers727502773
pharmgkbrs727502773
gwascentralrs727502773
openSNPrs727502773
23andMers727502773
23andMe allrs727502773
SNP Nexus

SNPshotrs727502773
SNPdbers727502773
MSV3drs727502773
GWAS Ctlgrs727502773
Max Magnitude0
ClinVar
Risk rs727502773(AG;AG)
Alt rs727502773(AG;AG)
Reference rs727502773(;)
Significance Pathogenic
Disease Epilepsy not provided
Variation info
Gene SCARB2
CLNDBN Epilepsy, progressive myoclonic 4, with or without renal failure not provided
Reversed 1
HGVS NC_000004.11:g.77100847_77100848dupCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000007802.3, RCV000188810.1,