Have questions? Visit https://www.reddit.com/r/SNPedia

rs757011098

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757011098(A;A)
Make rs757011098(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position75106541
GeneNEK9
is asnp
is mentioned by
dbSNPrs757011098
ebirs757011098
HLIrs757011098
Exacrs757011098
Varsomers757011098
Maprs757011098
PheGenIrs757011098
hapmaprs757011098
1000 genomesrs757011098
hgdprs757011098
ensemblrs757011098
gopubmedrs757011098
geneviewrs757011098
scholarrs757011098
googlers757011098
pharmgkbrs757011098
gwascentralrs757011098
openSNPrs757011098
23andMers757011098
23andMe allrs757011098
SNP Nexus

SNPshotrs757011098
SNPdbers757011098
MSV3drs757011098
GWAS Ctlgrs757011098
Max Magnitude0
ClinVar
Risk rs757011098(A;A)
Alt rs757011098(A;A)
Reference rs757011098(G;G)
Significance Pathogenic
Disease Lethal congenital contracture syndrome 10
Variation info
Gene NEK9
CLNDBN Lethal congenital contracture syndrome 10
Reversed 0
HGVS NC_000014.8:g.75573244G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000234925.1,