rs61664582

Orientation

minus

Stabilized

minus

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

Make rs61664582(G;T)

Make rs61664582(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

41583278

Gene

KRT14

is a	snp
is	mentioned by
dbSNP	rs61664582
dbSNP (classic)	rs61664582
ClinGen	rs61664582
ebi	rs61664582
HLI	rs61664582
Exac	rs61664582
Gnomad	rs61664582
Varsome	rs61664582
LitVar	rs61664582
Map	rs61664582
PheGenI	rs61664582
Biobank	rs61664582
1000 genomes	rs61664582
hgdp	rs61664582
ensembl	rs61664582
geneview	rs61664582
scholar	rs61664582
google	rs61664582
pharmgkb	rs61664582
gwascentral	rs61664582
openSNP	rs61664582
23andMe	rs61664582
SNPshot	rs61664582
SNPdbe	rs61664582
MSV3d	rs61664582
GWAS Ctlg	rs61664582

Max Magnitude

0

ClinVar
Risk	rs61664582(A;A) rs61664582(T;T)
Alt	rs61664582(A;A) rs61664582(T;T)
Reference	Rs61664582(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRT14
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.39739530C>A; NC_000017.10:g.39739530C>T
CLNSRC
CLNACC	RCV000056678.1, RCV000056677.2,