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rs864321666

From SNPedia

Orientationminus
Make rs864321666(-;-)
Make rs864321666(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position27182866
GeneHOXA11
is asnp
is mentioned by
dbSNPrs864321666
ebirs864321666
HLIrs864321666
Exacrs864321666
Varsomers864321666
Maprs864321666
PheGenIrs864321666
hapmaprs864321666
1000 genomesrs864321666
hgdprs864321666
ensemblrs864321666
gopubmedrs864321666
geneviewrs864321666
scholarrs864321666
googlers864321666
pharmgkbrs864321666
gwascentralrs864321666
openSNPrs864321666
23andMers864321666
23andMe allrs864321666
SNP Nexus

SNPshotrs864321666
SNPdbers864321666
MSV3drs864321666
GWAS Ctlgrs864321666
Max Magnitude
ClinVar
Risk rs864321666(;)
Alt rs864321666(;)
Reference rs864321666(A;A)
Significance Pathogenic
Disease Radioulnar synostosis with amegakaryocytic thrombocytopenia
Variation info
Gene HOXA11
CLNDBN Radioulnar synostosis with amegakaryocytic thrombocytopenia
Reversed 1
HGVS NC_000007.13:g.27222485delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000016026.22,