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rs398124552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398124552(-;-)
Make rs398124552(-;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position145655211
GeneMMAA
is asnp
is mentioned by
dbSNPrs398124552
ebirs398124552
HLIrs398124552
Exacrs398124552
Varsomers398124552
Maprs398124552
PheGenIrs398124552
hapmaprs398124552
1000 genomesrs398124552
hgdprs398124552
ensemblrs398124552
gopubmedrs398124552
geneviewrs398124552
scholarrs398124552
googlers398124552
pharmgkbrs398124552
gwascentralrs398124552
openSNPrs398124552
23andMers398124552
23andMe allrs398124552
SNP Nexus

SNPshotrs398124552
SNPdbers398124552
MSV3drs398124552
GWAS Ctlgrs398124552
Max Magnitude0
ClinVar
Risk rs398124552(;)
Alt rs398124552(;)
Reference rs398124552(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MMAA
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.146576363delT
CLNSRC ClinVar
CLNACC RCV000082687.4,