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rs606231260

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231260(A;G)
Make rs606231260(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position37201810
GeneC5orf42
is asnp
is mentioned by
dbSNPrs606231260
ebirs606231260
HLIrs606231260
Exacrs606231260
Varsomers606231260
Maprs606231260
PheGenIrs606231260
hapmaprs606231260
1000 genomesrs606231260
hgdprs606231260
ensemblrs606231260
gopubmedrs606231260
geneviewrs606231260
scholarrs606231260
googlers606231260
pharmgkbrs606231260
gwascentralrs606231260
openSNPrs606231260
23andMers606231260
23andMe allrs606231260
SNP Nexus

SNPshotrs606231260
SNPdbers606231260
MSV3drs606231260
GWAS Ctlgrs606231260
Max Magnitude0
ClinVar
Risk rs606231260(G;G)
Alt rs606231260(G;G)
Reference rs606231260(A;A)
Significance Pathogenic
Disease Orofaciodigital syndrome 6
Variation info
Gene C5orf42
CLNDBN Orofaciodigital syndrome 6
Reversed 1
HGVS NC_000005.9:g.37201912T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000144859.3,