95525015
3:46902543
3:46902543
G
C/G/T
Not specified
Not specified
-
SNP
dbSNP
Frequency~Cited~Phenotype_or_Disease~ExAC~gnomAD
pathogenic
missense variant
T/R
410
410
11
deleterious
1
1001
probably damaging
1
28001
likely benign
28
503
likely disease causing
502
359
tolerated
358
982
high
981
ENST00000313049.9

Creators
Not specifiedSubmitter
Views: 127
Created: 16th Jun 2021 at 11:05

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