rs61027685

Orientation

minus

Stabilized

minus

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

Make rs61027685(G;T)

Make rs61027685(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

41586438

Gene

KRT14

is a	snp
is	mentioned by
dbSNP	rs61027685
dbSNP (classic)	rs61027685
ClinGen	rs61027685
ebi	rs61027685
HLI	rs61027685
Exac	rs61027685
Gnomad	rs61027685
Varsome	rs61027685
LitVar	rs61027685
Map	rs61027685
PheGenI	rs61027685
Biobank	rs61027685
1000 genomes	rs61027685
hgdp	rs61027685
ensembl	rs61027685
geneview	rs61027685
scholar	rs61027685
google	rs61027685
pharmgkb	rs61027685
gwascentral	rs61027685
openSNP	rs61027685
23andMe	rs61027685
SNPshot	rs61027685
SNPdbe	rs61027685
MSV3d	rs61027685
GWAS Ctlg	rs61027685

Max Magnitude

0

ClinVar
Risk	rs61027685(A;A) rs61027685(C;C) rs61027685(T;T)
Alt	rs61027685(A;A) rs61027685(C;C) rs61027685(T;T)
Reference	Rs61027685(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRT14
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.39742690C>A; NC_000017.10:g.39742690C>G; NC_000017.10:g.39742690C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056729.1, RCV000056728.1, RCV000056727.2,