Most severe consequence
13
missense variant
Alleles
G/A|Ancestral: G
Change tolerance
CADD: A:26.6
Location
Chromosome X:107821549 (forward strand)|VCF:X 107821549 rs104886068 G A
Co-located variant
HGMD-PUBLIC CM960344
Evidence status 
HGVS names
This variant has 5 HGVS names - Show
Synonyms
This variant has 2 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 and is mentioned in 1 citation.
Description from SNPedia
Description not available [More information from SNPedia]