rs797044886

Orientation

minus

Stabilized

minus

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

Make rs797044886(A;A)

Make rs797044886(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

153950387

Gene

HCFC1

is a	snp
is	mentioned by
dbSNP	rs797044886
dbSNP (classic)	rs797044886
ClinGen	rs797044886
ebi	rs797044886
HLI	rs797044886
Exac	rs797044886
Gnomad	rs797044886
Varsome	rs797044886
LitVar	rs797044886
Map	rs797044886
PheGenI	rs797044886
Biobank	rs797044886
1000 genomes	rs797044886
hgdp	rs797044886
ensembl	rs797044886
geneview	rs797044886
scholar	rs797044886
google	rs797044886
pharmgkb	rs797044886
gwascentral	rs797044886
openSNP	rs797044886
23andMe	rs797044886
SNPshot	rs797044886
SNPdbe	rs797044886
MSV3d	rs797044886
GWAS Ctlg	rs797044886

Max Magnitude

0

ClinVar
Risk	rs797044886(A;A)
Alt	rs797044886(A;A)
Reference	Rs797044886(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	HCFC1
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000023.10:g.153215838C>T
CLNSRC
CLNACC	RCV000190708.1,