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rs876657374

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657374(-;-)
Make rs876657374(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position119677732
GeneNECTIN1
is asnp
is mentioned by
dbSNPrs876657374
ebirs876657374
HLIrs876657374
Exacrs876657374
Varsomers876657374
Maprs876657374
PheGenIrs876657374
hapmaprs876657374
1000 genomesrs876657374
hgdprs876657374
ensemblrs876657374
gopubmedrs876657374
geneviewrs876657374
scholarrs876657374
googlers876657374
pharmgkbrs876657374
gwascentralrs876657374
openSNPrs876657374
23andMers876657374
23andMe allrs876657374
SNP Nexus

SNPshotrs876657374
SNPdbers876657374
MSV3drs876657374
GWAS Ctlgrs876657374
Max Magnitude0
ClinVar
Risk rs876657374(;)
Alt rs876657374(;)
Reference rs876657374(G;G)
Significance Pathogenic
Disease Cleft lip/palate-ectodermal dysplasia syndrome
Variation info
Gene PVRL1
CLNDBN Cleft lip/palate-ectodermal dysplasia syndrome
Reversed 1
HGVS NC_000011.9:g.119548442delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000009533.4,