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rs61973742

From SNPedia

Orientationplus
Make rs61973742(A;A)
Make rs61973742(A;G)
Make rs61973742(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position101430922
is asnp
is mentioned by
dbSNPrs61973742
ebirs61973742
HLIrs61973742
Exacrs61973742
Varsomers61973742
Maprs61973742
PheGenIrs61973742
hapmaprs61973742
1000 genomesrs61973742
hgdprs61973742
ensemblrs61973742
gopubmedrs61973742
geneviewrs61973742
scholarrs61973742
googlers61973742
pharmgkbrs61973742
gwascentralrs61973742
openSNPrs61973742
23andMers61973742
23andMe allrs61973742
SNP Nexus

SNPshotrs61973742
SNPdbers61973742
MSV3drs61973742
GWAS Ctlgrs61973742
Max Magnitude

[PMID 25256078] Lack of validation of variants associated with cervical dystonia risk: a GWAS replication study