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rs149428

From SNPedia

Orientationplus
Stabilizedplus
Make rs149428(A;A)
Make rs149428(A;G)
Make rs149428(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position58634662
is asnp
is mentioned by
dbSNPrs149428
ebirs149428
HLIrs149428
Exacrs149428
Varsomers149428
Maprs149428
PheGenIrs149428
hapmaprs149428
1000 genomesrs149428
hgdprs149428
ensemblrs149428
gopubmedrs149428
geneviewrs149428
scholarrs149428
googlers149428
pharmgkbrs149428
gwascentralrs149428
openSNPrs149428
23andMers149428
23andMe allrs149428
SNP Nexus

SNPshotrs149428
SNPdbers149428
MSV3drs149428
GWAS Ctlgrs149428
GMAF0.1983
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM612319
DescSPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE; SPG35
Variant
Relatedalso

[PMID 18463364] A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.