rs3826550

Orientation

plus

Stabilized

plus

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

Make rs3826550(C;T)

Make rs3826550(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

41586555

Gene

KRT14

is a	snp
is	mentioned by
dbSNP	rs3826550
dbSNP (classic)	rs3826550
ClinGen	rs3826550
ebi	rs3826550
HLI	rs3826550
Exac	rs3826550
Gnomad	rs3826550
Varsome	rs3826550
LitVar	rs3826550
Map	rs3826550
PheGenI	rs3826550
Biobank	rs3826550
1000 genomes	rs3826550
hgdp	rs3826550
ensembl	rs3826550
geneview	rs3826550
scholar	rs3826550
google	rs3826550
pharmgkb	rs3826550
gwascentral	rs3826550
openSNP	rs3826550
23andMe	rs3826550
SNPshot	rs3826550
SNPdbe	rs3826550
MSV3d	rs3826550
GWAS Ctlg	rs3826550

GMAF

0.2984

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

ClinVar
Risk	rs3826550(T;T)
Alt	rs3826550(T;T)
Reference	Rs3826550(C;C)
Significance	Non-pathogenic
Disease	not provided not specified
Variation	info
Gene	KRT14
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000017.10:g.39742807C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056702.1, RCV000248897.1,