Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.41 (G)
Location

Chromosome X:91393737 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57853802

This variation has 8 HGVS names - click the plus to show

X:g.91393737A>G
ENST00000406881.1:c.3034-62637A>G
ENST00000373097.1:c.3034-62637A>G
ENST00000373094.1:c.3034-62637A>G
ENST00000361655.2:c.3034-62637A>G
ENST00000373088.1:c.3034-248997A>G
ENST00000504220.2:c.3034-62637A>G
ENST00000298274.8:c.3034-248997A>G

This variation has assays on 8 chips - click the plus to show

Variation displays