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rs17586672

From SNPedia

Orientationplus
Stabilizedplus
Make rs17586672(C;C)
Make rs17586672(C;T)
Make rs17586672(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position23941518
is asnp
is mentioned by
dbSNPrs17586672
dbSNP (old)rs17586672
ClinGenrs17586672
ebirs17586672
HLIrs17586672
Exacrs17586672
Gnomadrs17586672
Varsomers17586672
LitVarrs17586672
Maprs17586672
PheGenIrs17586672
Biobankrs17586672
1000 genomesrs17586672
hgdprs17586672
ensemblrs17586672
gopubmedrs17586672
geneviewrs17586672
scholarrs17586672
googlers17586672
pharmgkbrs17586672
gwascentralrs17586672
openSNPrs17586672
23andMers17586672
23andMe allrs17586672
SNPshotrs17586672
SNPdbers17586672
MSV3drs17586672
GWAS Ctlgrs17586672
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 28289475OA-icon.png] Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families.