rs387906896

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs387906896(C;T)

Make rs387906896(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160349583

Gene

NCSTN

is a	snp
is	mentioned by
dbSNP	rs387906896
dbSNP (classic)	rs387906896
ClinGen	rs387906896
ebi	rs387906896
HLI	rs387906896
Exac	rs387906896
Gnomad	rs387906896
Varsome	rs387906896
LitVar	rs387906896
Map	rs387906896
PheGenI	rs387906896
Biobank	rs387906896
1000 genomes	rs387906896
hgdp	rs387906896
ensembl	rs387906896
geneview	rs387906896
scholar	rs387906896
google	rs387906896
pharmgkb	rs387906896
gwascentral	rs387906896
openSNP	rs387906896
23andMe	rs387906896
SNPshot	rs387906896
SNPdbe	rs387906896
MSV3d	rs387906896
GWAS Ctlg	rs387906896

Max Magnitude

0

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,