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

rs797045100

From SNPedia

Orientationminus
Make rs797045100(-;-)
Make rs797045100(-;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position13283751
GenePHYH
is asnp
is mentioned by
dbSNPrs797045100
ebirs797045100
HLIrs797045100
Exacrs797045100
Varsomers797045100
Maprs797045100
PheGenIrs797045100
hapmaprs797045100
1000 genomesrs797045100
hgdprs797045100
ensemblrs797045100
gopubmedrs797045100
geneviewrs797045100
scholarrs797045100
googlers797045100
pharmgkbrs797045100
gwascentralrs797045100
openSNPrs797045100
23andMers797045100
23andMe allrs797045100
SNP Nexus

SNPshotrs797045100
SNPdbers797045100
MSV3drs797045100
GWAS Ctlgrs797045100
Max Magnitude
ClinVar
Risk rs797045100(;)
Alt rs797045100(;)
Reference rs797045100(GT;GT)
Significance Probable-Pathogenic
Disease Phytanic acid storage disease
Variation info
Gene PHYH
CLNDBN Phytanic acid storage disease
Reversed 1
HGVS NC_000010.10:g.13325751_13325752delAC
CLNSRC
CLNACC RCV000190614.1,