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rs2246786

From SNPedia

Orientationplus
Stabilizedplus
Make rs2246786(A;A)
Make rs2246786(A;G)
Make rs2246786(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position95411361
is asnp
is mentioned by
dbSNPrs2246786
dbSNP (classic)rs2246786
ClinGenrs2246786
ebirs2246786
HLIrs2246786
Exacrs2246786
Gnomadrs2246786
Varsomers2246786
LitVarrs2246786
Maprs2246786
PheGenIrs2246786
Biobankrs2246786
1000 genomesrs2246786
hgdprs2246786
ensemblrs2246786
geneviewrs2246786
scholarrs2246786
googlers2246786
pharmgkbrs2246786
gwascentralrs2246786
openSNPrs2246786
23andMers2246786
SNPshotrs2246786
SNPdbers2246786
MSV3drs2246786
GWAS Ctlgrs2246786
GMAF0.1983
Max Magnitude0
? (A;A) (A;G) (G;G) 28


OMIM611092
DescMENTAL RETARDATION, AUTOSOMAL RECESSIVE 6; MRT6
Variant
Relatedalso