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rs150911354

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150911354(C;T)
Make rs150911354(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64747224
GenePYGM, RASGRP2
is asnp
is mentioned by
dbSNPrs150911354
dbSNP (classic)rs150911354
ClinGenrs150911354
ebirs150911354
HLIrs150911354
Exacrs150911354
Gnomadrs150911354
Varsomers150911354
LitVarrs150911354
Maprs150911354
PheGenIrs150911354
Biobankrs150911354
1000 genomesrs150911354
hgdprs150911354
ensemblrs150911354
geneviewrs150911354
scholarrs150911354
googlers150911354
pharmgkbrs150911354
gwascentralrs150911354
openSNPrs150911354
23andMers150911354
23andMe allrs150911354
SNPshotrs150911354
SNPdbers150911354
MSV3drs150911354
GWAS Ctlgrs150911354
Max Magnitude0
ClinVar
Risk rs150911354(T;T)
Alt rs150911354(T;T)
Reference Rs150911354(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PYGM RASGRP2
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.64514696C>T
CLNSRC
CLNACC RCV000493384.1,