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rs730882195

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882195(C;C)
Make rs730882195(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position60114271
GeneANK3
is asnp
is mentioned by
dbSNPrs730882195
ebirs730882195
HLIrs730882195
Exacrs730882195
Varsomers730882195
Maprs730882195
PheGenIrs730882195
hapmaprs730882195
1000 genomesrs730882195
hgdprs730882195
ensemblrs730882195
gopubmedrs730882195
geneviewrs730882195
scholarrs730882195
googlers730882195
pharmgkbrs730882195
gwascentralrs730882195
openSNPrs730882195
23andMers730882195
23andMe allrs730882195
SNP Nexus

SNPshotrs730882195
SNPdbers730882195
MSV3drs730882195
GWAS Ctlgrs730882195
Max Magnitude0
ClinVar
Risk rs730882195(C;C)
Alt rs730882195(C;C)
Reference rs730882195(G;G)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene ANK3
CLNDBN Mental retardation, autosomal recessive 37
Reversed 1
HGVS NC_000010.10:g.61874029C>G
CLNSRC
CLNACC RCV000162096.1,