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rs730882213

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882213(A;A)
Make rs730882213(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1912477
GeneADAT3, SCAMP4
is asnp
is mentioned by
dbSNPrs730882213
ebirs730882213
HLIrs730882213
Exacrs730882213
Varsomers730882213
Maprs730882213
PheGenIrs730882213
hapmaprs730882213
1000 genomesrs730882213
hgdprs730882213
ensemblrs730882213
gopubmedrs730882213
geneviewrs730882213
scholarrs730882213
googlers730882213
pharmgkbrs730882213
gwascentralrs730882213
openSNPrs730882213
23andMers730882213
23andMe allrs730882213
SNP Nexus

SNPshotrs730882213
SNPdbers730882213
MSV3drs730882213
GWAS Ctlgrs730882213
Max Magnitude0
ClinVar
Risk rs730882213(A;A)
Alt rs730882213(A;A)
Reference rs730882213(G;G)
Significance Other
Disease Mental retardation
Variation info
Gene ADAT3 SCAMP4
CLNDBN Mental retardation, autosomal recessive 36
Reversed 0
HGVS NC_000019.9:g.1912476G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000162122.2,