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rs876657388

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657388(A;A)
Make rs876657388(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position147539823
GeneEDNRA
is asnp
is mentioned by
dbSNPrs876657388
ebirs876657388
HLIrs876657388
Exacrs876657388
Varsomers876657388
Maprs876657388
PheGenIrs876657388
hapmaprs876657388
1000 genomesrs876657388
hgdprs876657388
ensemblrs876657388
gopubmedrs876657388
geneviewrs876657388
scholarrs876657388
googlers876657388
pharmgkbrs876657388
gwascentralrs876657388
openSNPrs876657388
23andMers876657388
23andMe allrs876657388
SNP Nexus

SNPshotrs876657388
SNPdbers876657388
MSV3drs876657388
GWAS Ctlgrs876657388
Max Magnitude0
ClinVar
Risk rs876657388(A;A)
Alt rs876657388(A;A)
Reference rs876657388(G;G)
Significance Pathogenic
Disease Mandibulofacial dysostosis with alopecia
Variation info
Gene EDNRA
CLNDBN Mandibulofacial dysostosis with alopecia
Reversed 0
HGVS NC_000004.11:g.148460975G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000170510.3,