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rs876657384

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657384(-;-)
Make rs876657384(-;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position47142407
GeneNDUFB11
is asnp
is mentioned by
dbSNPrs876657384
ebirs876657384
HLIrs876657384
Exacrs876657384
Varsomers876657384
Maprs876657384
PheGenIrs876657384
hapmaprs876657384
1000 genomesrs876657384
hgdprs876657384
ensemblrs876657384
gopubmedrs876657384
geneviewrs876657384
scholarrs876657384
googlers876657384
pharmgkbrs876657384
gwascentralrs876657384
openSNPrs876657384
23andMers876657384
23andMe allrs876657384
SNP Nexus

SNPshotrs876657384
SNPdbers876657384
MSV3drs876657384
GWAS Ctlgrs876657384
Max Magnitude0
ClinVar
Risk rs876657384(;)
Alt rs876657384(;)
Reference rs876657384(G;G)
Significance Pathogenic
Disease Linear skin defects with multiple congenital anomalies 3
Variation info
Gene NDUFB11
CLNDBN Linear skin defects with multiple congenital anomalies 3
Reversed 1
HGVS NC_000023.10:g.47001806delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000170491.3,