rs267607477

Orientation

minus

Stabilized

minus

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

Make rs267607477(A;A)

Make rs267607477(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

52567115

Gene

KRT74

is a	snp
is	mentioned by
dbSNP	rs267607477
dbSNP (classic)	rs267607477
ClinGen	rs267607477
ebi	rs267607477
HLI	rs267607477
Exac	rs267607477
Gnomad	rs267607477
Varsome	rs267607477
LitVar	rs267607477
Map	rs267607477
PheGenI	rs267607477
Biobank	rs267607477
1000 genomes	rs267607477
hgdp	rs267607477
ensembl	rs267607477
geneview	rs267607477
scholar	rs267607477
google	rs267607477
pharmgkb	rs267607477
gwascentral	rs267607477
openSNP	rs267607477
23andMe	rs267607477
SNPshot	rs267607477
SNPdbe	rs267607477
MSV3d	rs267607477
GWAS Ctlg	rs267607477

Max Magnitude

0

ClinVar
Risk	rs267607477(A;A)
Alt	rs267607477(A;A)
Reference	Rs267607477(G;G)
Significance	Pathogenic
Disease	Hypotrichosis 3 not provided
Variation	info
Gene	KRT74
CLNDBN	Hypotrichosis 3 not provided
Reversed	1
HGVS	NC_000012.11:g.52960899C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023697.6, RCV000057502.1,