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: 0.34 (G)
Location

Chromosome 16:23622705 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 6 HGVS names - click the plus to show

16:g.23622705A>G
ENST00000568219.3:c.*2871+264T>C
ENST00000561764.1:n.420-1195A>G
ENST00000261584.6:c.2996+264T>C
LRG_308:g.23653T>C
LRG_308t1:c.2996+264T>C

This variation has assays on 14 chips - click the plus to show

Variation displays