Have questions? Visit https://www.reddit.com/r/SNPedia

rs797044886

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044886(A;A)
Make rs797044886(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153950387
GeneHCFC1
is asnp
is mentioned by
dbSNPrs797044886
ebirs797044886
HLIrs797044886
Exacrs797044886
Varsomers797044886
Maprs797044886
PheGenIrs797044886
hapmaprs797044886
1000 genomesrs797044886
hgdprs797044886
ensemblrs797044886
gopubmedrs797044886
geneviewrs797044886
scholarrs797044886
googlers797044886
pharmgkbrs797044886
gwascentralrs797044886
openSNPrs797044886
23andMers797044886
23andMe allrs797044886
SNP Nexus

SNPshotrs797044886
SNPdbers797044886
MSV3drs797044886
GWAS Ctlgrs797044886
Max Magnitude0
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,