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rs730882163

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882163(A;A)
Make rs730882163(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position104802387
GeneZBTB42
is asnp
is mentioned by
dbSNPrs730882163
ebirs730882163
HLIrs730882163
Exacrs730882163
Varsomers730882163
Maprs730882163
PheGenIrs730882163
hapmaprs730882163
1000 genomesrs730882163
hgdprs730882163
ensemblrs730882163
gopubmedrs730882163
geneviewrs730882163
scholarrs730882163
googlers730882163
pharmgkbrs730882163
gwascentralrs730882163
openSNPrs730882163
23andMers730882163
23andMe allrs730882163
SNP Nexus

SNPshotrs730882163
SNPdbers730882163
MSV3drs730882163
GWAS Ctlgrs730882163
Max Magnitude0
ClinVar
Risk rs730882163(A;A)
Alt rs730882163(A;A)
Reference rs730882163(G;G)
Significance Pathogenic
Disease Lethal congenital contracture syndrome 6
Variation info
Gene ZBTB42
CLNDBN Lethal congenital contracture syndrome 6
Reversed 0
HGVS NC_000014.8:g.105268724G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000162044.4,