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rs2866413

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 0
(G;G) 0 common in clinvar


Make rs2866413(A;A)
ReferenceGRCh38 38.1/141
Chromosome4
Position102635920
GeneMANBA
is asnp
is mentioned by
dbSNPrs2866413
dbSNP (classic)rs2866413
ClinGenrs2866413
ebirs2866413
HLIrs2866413
Exacrs2866413
Gnomadrs2866413
Varsomers2866413
LitVarrs2866413
Maprs2866413
PheGenIrs2866413
Biobankrs2866413
1000 genomesrs2866413
hgdprs2866413
ensemblrs2866413
geneviewrs2866413
scholarrs2866413
googlers2866413
pharmgkbrs2866413
gwascentralrs2866413
openSNPrs2866413
23andMers2866413
SNPshotrs2866413
SNPdbers2866413
MSV3drs2866413
GWAS Ctlgrs2866413
GMAF0.449
Max Magnitude0
? (A;A) (A;G) (G;G) 28




ClinVar
Risk rs2866413(A;A) rs2866413(C;C)
Alt rs2866413(A;A) rs2866413(C;C)
Reference Rs2866413(G;G)
Significance Non-pathogenic
Disease not specified Beta-D-mannosidosis
Variation info
Gene MANBA
CLNDBN not specified Beta-D-mannosidosis
Reversed 0
HGVS NC_000004.11:g.103557077G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000081336.4, RCV000403534.1,