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rs1998463

From SNPedia

Orientationplus
Stabilizedplus
Make rs1998463(C;C)
Make rs1998463(C;G)
Make rs1998463(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position27039812
is asnp
is mentioned by
dbSNPrs1998463
ebirs1998463
HLIrs1998463
Exacrs1998463
Varsomers1998463
Maprs1998463
PheGenIrs1998463
hapmaprs1998463
1000 genomesrs1998463
hgdprs1998463
ensemblrs1998463
gopubmedrs1998463
geneviewrs1998463
scholarrs1998463
googlers1998463
pharmgkbrs1998463
gwascentralrs1998463
openSNPrs1998463
23andMers1998463
23andMe allrs1998463
SNP Nexus

SNPshotrs1998463
SNPdbers1998463
MSV3drs1998463
GWAS Ctlgrs1998463
GMAF0.3375
Max Magnitude
? (C;C) (C;G) (G;G) 28
OMIM611095
DescMENTAL RETARDATION, AUTOSOMAL RECESSIVE 9; MRT9
Variant
Relatedalso