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 (A)
Location

Chromosome 17:66435948 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59935790

This variation has 4 HGVS names - click the plus to show

17:g.66435948A>G
ENST00000413366.5:c.206-60253A>G
ENST00000578063.3:c.206-60253A>G
ENST00000284384.6:c.198-60253A>G

This variation has assays on 9 chips - click the plus to show

Variation displays