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rs375009168

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs375009168(G;T)
Make rs375009168(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position37201718
GeneC5orf42
is asnp
is mentioned by
dbSNPrs375009168
ebirs375009168
HLIrs375009168
Exacrs375009168
Varsomers375009168
Maprs375009168
PheGenIrs375009168
hapmaprs375009168
1000 genomesrs375009168
hgdprs375009168
ensemblrs375009168
gopubmedrs375009168
geneviewrs375009168
scholarrs375009168
googlers375009168
pharmgkbrs375009168
gwascentralrs375009168
openSNPrs375009168
23andMers375009168
23andMe allrs375009168
SNP Nexus

SNPshotrs375009168
SNPdbers375009168
MSV3drs375009168
GWAS Ctlgrs375009168
Max Magnitude0
ClinVar
Risk rs375009168(A,T;A,T)
Alt rs375009168(A,T;A,T)
Reference rs375009168(G;G)
Significance Pathogenic
Disease Orofaciodigital syndrome 6
Variation info
Gene C5orf42
CLNDBN Orofaciodigital syndrome 6
Reversed 0
HGVS NC_000005.9:g.37201820G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144860.3,