Most severe consequence
13
missense variant
Alleles
G/A/T|Ancestral: G
Change tolerance
CADD: A:26.9, T:28.7
Location
Chromosome X:107819167 (forward strand)|VCF:X 107819167 rs104886060 G A,T
Co-located variant
HGMD-PUBLIC CM010190
Evidence status 
Clinical significance
HGVS names
This variant has 10 HGVS names - Show
Synonyms
This variant has 5 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant overlaps 2 transcripts, is associated with 3 phenotypes and is mentioned in 1 citation.
Description from SNPedia
Description not available [More information from SNPedia]