rs267606775

Orientation

plus

Stabilized

plus

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

Make rs267606775(C;C)

Make rs267606775(C;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31390712

Gene	DSG1-AS1, DSG4

is a	snp
is	mentioned by
dbSNP	rs267606775
dbSNP (classic)	rs267606775
ClinGen	rs267606775
ebi	rs267606775
HLI	rs267606775
Exac	rs267606775
Gnomad	rs267606775
Varsome	rs267606775
LitVar	rs267606775
Map	rs267606775
PheGenI	rs267606775
Biobank	rs267606775
1000 genomes	rs267606775
hgdp	rs267606775
ensembl	rs267606775
geneview	rs267606775
scholar	rs267606775
google	rs267606775
pharmgkb	rs267606775
gwascentral	rs267606775
openSNP	rs267606775
23andMe	rs267606775
SNPshot	rs267606775
SNPdbe	rs267606775
MSV3d	rs267606775
GWAS Ctlg	rs267606775

Max Magnitude

0

ClinVar
Risk	rs267606775(A;A) rs267606775(C;C)
Alt	rs267606775(A;A) rs267606775(C;C)
Reference	Rs267606775(T;T)
Significance	Pathogenic
Disease	Hypotrichosis 6
Variation	info
Gene	DSG1-AS1 DSG4
CLNDBN	Hypotrichosis 6
Reversed	0
HGVS	NC_000018.9:g.28970675T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002840.3,