Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.42 (G)
Location

Chromosome X:92138738 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57853802

HGVS names

This variant has 7 HGVS names - Hide

X:g.92138738A>G
ENST00000406881.3:c.3034-62637A>G
ENST00000373094.5:c.3034-62637A>G
ENST00000373097.5:c.3034-62637A>G
ENST00000361655.6:c.3034-62637A>G
ENST00000373088.5:c.3034-248997A>G
ENST00000504220.6:c.3034-62637A>G

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 6 transcripts, has 3683 sample genotypes and is mentioned in 14 citations.

Variant displays