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rs1313770

From SNPedia

Orientationplus
Stabilizedplus
Make rs1313770(A;A)
Make rs1313770(A;G)
Make rs1313770(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position3056082
is asnp
is mentioned by
dbSNPrs1313770
ebirs1313770
HLIrs1313770
Exacrs1313770
Varsomers1313770
Maprs1313770
PheGenIrs1313770
hapmaprs1313770
1000 genomesrs1313770
hgdprs1313770
ensemblrs1313770
gopubmedrs1313770
geneviewrs1313770
scholarrs1313770
googlers1313770
pharmgkbrs1313770
gwascentralrs1313770
openSNPrs1313770
23andMers1313770
23andMe allrs1313770
SNP Nexus

SNPshotrs1313770
SNPdbers1313770
MSV3drs1313770
GWAS Ctlgrs1313770
GMAF0.4614
Max Magnitude
OMIM143100
DescHUNTINGTON DISEASE; HD
Variant
Relatedalso


[PMID 15832309] Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.