Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57853802

This variation has 7 HGVS names - click the plus to show

X:g.92138738A>G
ENST00000406881.2:c.3034-62637A>G
ENST00000373097.2:c.3034-62637A>G
ENST00000373094.2:c.3034-62637A>G
ENST00000373088.2:c.3034-248997A>G
ENST00000361655.3:c.3034-62637A>G
ENST00000504220.3:c.3034-62637A>G

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

Variation displays