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

rs794726673

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794726673(-;-)
Make rs794726673(-;G)
Make rs794726673(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position54727449
GeneKIT
is asnp
is mentioned by
dbSNPrs794726673
ebirs794726673
HLIrs794726673
Exacrs794726673
Varsomers794726673
Maprs794726673
PheGenIrs794726673
hapmaprs794726673
1000 genomesrs794726673
hgdprs794726673
ensemblrs794726673
gopubmedrs794726673
geneviewrs794726673
scholarrs794726673
googlers794726673
pharmgkbrs794726673
gwascentralrs794726673
openSNPrs794726673
23andMers794726673
23andMe allrs794726673
SNP Nexus

SNPshotrs794726673
SNPdbers794726673
MSV3drs794726673
GWAS Ctlgrs794726673
Max Magnitude0
ClinVar
Risk rs794726673(G;G)
Alt rs794726673(G;G)
Reference rs794726673(;)
Significance Pathogenic
Disease Partial albinism
Variation info
Gene KIT
CLNDBN Partial albinism
Reversed 0
HGVS NC_000004.11:g.55593615dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000014860.26,