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: 0.38 (A)
Location

Chromosome 1:206770888 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61317010

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

1:g.206770888A>G
ENST00000367099.3:n.283+19T>C
ENST00000471071.1:n.293+19T>C
ENST00000423557.1:c.378+19T>C

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

Variation displays