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rs387906896

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906896(C;T)
Make rs387906896(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160349583
GeneNCSTN
is asnp
is mentioned by
dbSNPrs387906896
ebirs387906896
HLIrs387906896
Exacrs387906896
Varsomers387906896
Maprs387906896
PheGenIrs387906896
hapmaprs387906896
1000 genomesrs387906896
hgdprs387906896
ensemblrs387906896
gopubmedrs387906896
geneviewrs387906896
scholarrs387906896
googlers387906896
pharmgkbrs387906896
gwascentralrs387906896
openSNPrs387906896
23andMers387906896
23andMe allrs387906896
SNP Nexus

SNPshotrs387906896
SNPdbers387906896
MSV3drs387906896
GWAS Ctlgrs387906896
Max Magnitude0
ClinVar
Risk rs387906896(T;T)
Alt rs387906896(T;T)
Reference rs387906896(C;C)
Significance Pathogenic
Disease Familial acne inversa 1
Variation info
Gene NCSTN
CLNDBN Familial acne inversa 1
Reversed 0
HGVS NC_000001.10:g.160319373C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023407.3,