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

rs796051991

From SNPedia

Orientationplus
Make rs796051991(-;-)
Make rs796051991(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position83899619
GeneMLYCD
is asnp
is mentioned by
dbSNPrs796051991
ebirs796051991
HLIrs796051991
Exacrs796051991
Varsomers796051991
Maprs796051991
PheGenIrs796051991
hapmaprs796051991
1000 genomesrs796051991
hgdprs796051991
ensemblrs796051991
gopubmedrs796051991
geneviewrs796051991
scholarrs796051991
googlers796051991
pharmgkbrs796051991
gwascentralrs796051991
openSNPrs796051991
23andMers796051991
23andMe allrs796051991
SNP Nexus

SNPshotrs796051991
SNPdbers796051991
MSV3drs796051991
GWAS Ctlgrs796051991
Max Magnitude
ClinVar
Risk rs796051991(;)
Alt rs796051991(;)
Reference rs796051991(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MLYCD
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.83933224delG
CLNSRC
CLNACC RCV000186010.1,