95524978
3:46902768
3:46902768
G
T/G
Not specified
Not specified
-
SNP
dbSNP
Frequency~Cited~Phenotype_or_Disease
pathogenic
missense variant
I/R
458
458
1
deleterious
0
991
probably damaging
99
31001
likely deleterious
31
635
likely disease causing
634
461
tolerated
46
801
medium
8
ENST00000313049.9

Creators
Not specifiedSubmitter
Views: 132
Created: 16th Jun 2021 at 11:05
Last updated: 16th Jun 2021 at 11:21

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